Публікації в міжнародних виданнях

2023 р.

Розділи в зарубіжних монографіях

• T.V. Tkachenko, D.S. Kamenskyh, Y.V. Sheludko, V.O. Yevdokymenko . Structural and morphological features of nanoсellulose from soybean straw. Nanoobjects & Nanostructuring. Volume I / Edited by Lidiya M. Boichyshyn and Oleksandr. V. Reshetnyak. ‒ Mississauga, Ontario: Nova Printing Inc. 2022. Р. 145-160.
• S. Konovalov, S. Zubenko, L. Patrylak, A. Yakovenko, V. Povazhnyi, K. Burlachenko. On the Peculiarities of Alkaline-Catalyzed Route of Synthesis of Fatty Acid Monoalkyl Esters. International Symposium on Electric Aircraft and Autonomous Systems.Advances in Electric Aviation.Р. 275-281.
• Patrylak L.K., Yakovenko A.V., Nizhnik B.O., Pertko O.P., Povazhnyi V.A., Kamenskyh D.S., Melnychuk O.V.. Natural Zeolites Modified with Silver Nanoparticles as Promising Sorbents with Antibacterial Properties. Nanoelectronics, Nanooptics, Nanochemistry and Nanobiotechnology, and Their Applications. Springer Proceedings in Physics. 2023. Р. 87-98.
• Tsygankova V.A.. Research Advances in Microbiology and Biotechnology. Book Publisher International. SCIENCEDO­MAIN international Ltd. India.United Kingdom. Vol. 3. 2023. 166 p. ISBN 978-81-19102-24-2 (Print) ISBN 978-81-19102-26-6 (eBook). DOI: 10.9734/bpi/ramb/v3.
• Tsygankova V.A.. Research Advances in Microbiology and Biotechnology. Book Publisher International. SCIENCEDOMAIN international Ltd. India.United Kingdom. Vol. 6. 2023. 183 p. ISBN 978-81-19315-43-7 (Print), ISBN 978-81-19315-40-6 (eBook). Р. 142-158DOI: 10.9734/bpi/ramb/v6.
• Tsygankova V.A.. Novel Aspects on Chemistry and Biochemistry. Book Publisher International. SCIENCEDOMAIN international Ltd. India.United Kingdom. Vol.1. 2023. 178 p. ISBN 978-81-19217-26-7 (Print), ISBN 978-81-19217-06-9 (eBook). Р. 1-8.DOI: 10.9734/bpi/nacb/v1.
• Tsygankova V.A.. Novel Aspects on Chemistry and Biochemistry. Book Publisher International. SCIENCEDOMAIN international Ltd. India.United Kingdom. Vol.4. 2023. 178 p. ISBN 978-81-19217-26-7 (Print), ISBN 978-81-19217-06-9 (eBook). Р. 13-24.DOI: 10.9734/bpi/nacb/v1.
• Tsygankova V.A., Spivak S.I., Shysha E.N., Pastukhova N.L., Biliavska L.A., Iutynska G.A., Kyrylenko V.M., Yemets A.I., Blume Ya.B.. The role of polycomponent biostimulants in increasing plant resistance to the biotic and abiotic stress factors. Chapter in Monograph: Agricultural Research Updates. Nova Science Publishers, Inc., NY, USA. 2023, Ed. Prathamesh Gorawala and Srushti Mandhatri, 307 p. ISBN 979-8-89113-332-7https://novapublishers.com/shop/agricultural-research-updates-volume-46/.

Публікації в зарубіжних виданнях

9. A.O. Kolodiazhna,O.I. Kolodiazhnyi. Chiral Organophosphorus drugs. Symmetry. 2023. V.15, N. 8. Р.1550. https://doi.org/10.3390/sym15081550
10. D. Kamenskyh, T. Tkachenko, L. Tecer, Y. Sheludko, V. Povazhny, M. Jafarov, V. Yevdokymenko. Influence of ratio of silicon complex and coagulant on silicon dioxide physicochemical characteristics. Applied Nanoscience. 2023. V. 13, N 10. P. 6967-6999. https://doi.org/10.1007/s13204-023-02841-2
11. M. Aksylenko, E. Sheludko, V. Yevdokymenko, O. Haidai, N. Khimach. Biostimulating Effect of Polygalacturonates of Biogenic Metals on Growing Winter Wheat. Cutting Edge Research in Biology. 2023. V. 6, N 11., Ch. 1. P. 1-24, https://doi.org/10.9734/bpi/cerb/v6/5047B
12. M.A. Jafarov, V.O. Yevdokymenko, D.S. Kamenskyh, K.A. Rustamov, Z.A. Jafarov. Mathematical Model Desublimation Conditions. Asian Journal of Chemical Sciences. 2023. V. 13, N 2. P. 1-6.https://doi.org/10.9734/AJOCS/2023/v13i2234
13. M.A. Jafarov, V.O. Yevdokymenko, D.S. Kamenskyh, K.A. Rustamov, Z.A. Jafarov. Mathematical Modeling of Hexafluorsilicate Ammonia Desublimation. Chemical Science International Journal. 2023. V. 32, N 3. P. 62-68. https://doi.org/10.9734/CSJI/2023/v32i3849
14. K. Hutsul, I. Ivanenko, L. Patrylak, O. Pertko, D. Kamenskyh. ZnO/Zeolite composite photocatalyst for dyes degradation. Applied Nanoscience. 2023. Р. 1-9. https://doi.org/10.1007/s13204-023-02950-y
15. M.A. Jafarov, V.O. Yevdokymenko, D.S. Kamenskyh, K.A. Rustamov, Z.A. Jafarov. Mathematical Modeling of Hexafluorsilicate Ammonia Desublimation. Evolutions Mech Eng. 2023. V. 4, N 4. EME.000595.2023. https://doi.org/10.31031/EME.2023.04.000595
16. Vretik L.O., Noskov Yu.V., Chepurna O.M., Ogurtsov N.A., O.A. Nikolaeva, O.A. Marynin, A.I. Ohulchanskyy, A.A. Pud . Dual Stimuli-Responsive Ternary Core-Shell Polystyrene@Pnipam-Pedot Latexes. Particle & Particle Systems Characterization. 2023. Р. 2300096. https://doi.org/10.1002/ppsc.202300096
17. Petrychuk M.V., Oliynyk V.V., Zagorodnii V.V.,Ogurtsov N.A., Pud A.A.. PVDF/poly(3-methylthiophene)/MWCNT nanocomposites for EMI shielding in the microwave range. Heliyon.2023. V. 9, N 12. Р. e23101
18. Z.I. Kazantseva, I.A. Koshets, A.V. Mamykin, A.S. Pavluchenko, O.L. Kukla, A.A. Pud, N.A. Ogurtsov, Yu.V. Noskov, R.V. Rodik, S.G. Vyshnevskyy. Detection of the explosive nitroaromatic compound simulants with chemosensory systems based on quartz crystal microbalance and chemiresistive sensor arrays. Semiconductor Physics, Quantum Electronics & Optoelectronics. 2023. V. 26, N.3. Р. 332-342
19. N. Redon, N. Davydenko, N. Ogurtsov, M. Jamar, Yu. Noskov, A. Pud, J.-L. Wojkiewicz. PPy & P3MT-MWCNT Nanocomposites-Based Sensors for Nerve Gas Detection at ppb Levels. 2023 IEEE SENSORS proceedings, 2023, Vienna, Austria. Р. 1-4.DOI: 10.1109/SENSORS56945.2023.10325230
20. I.P. Matushko, Yu.V. Noskov,V.A. Moiseienko,V.Y. Malyshev,L.M. Grishchenko. Electromagnetic Microwave Absorption Performances of PVC/AC Composites. Materials Proceedings. 2023. V. 14, N.1. Р. 15.https://doi.org/10.3390/IOCN2023-14537
21. D.О. Zhytnyk, I.P. Matushko, Yu.V. Noskov, V.A. Moiseienko, V.Yu. Malyshev, O.О. Barsukov, N.A. Atamas, L.M. Grishchenko. Microwave properties of composite materials based on PVC and oxidized activated carbon. Proceedings of the III International Scientific and Practical Conference “Science in the environment of rapid changes”, 2023, Brussels, Belgium. P. 237-244.
22. Kobzar O.L.,Tatarchuk, A.V.,Mrug G.P.,Bondarenko S.P., Demydchuk B.A., Frasinyuk M.S.,Vovk A.I.. Carboxylated chalcones and related flavonoids as inhibitors of xanthine oxidase. Medicinal Chemistry Research. 2023. V. 32, N 8. Р. 1804-1815
23. Velihina Y.,Gesese R.,Zhirnov V.,Kobzar O.,Bui B.,Pilyo S.,Vovk A.,Shen H.Brovarets V.. Design, synthesis and evaluation of the anti-breast cancer activity of 1,3-oxazolo[4, 5-d] pyrimidine and 1, 3-oxazolo[5, 4-d] pyrimidine derivatives. RSC Medicinal Chemistry. 2023. V. 14, N 4.Р. 692-699
24. Kovalishyn V.,Severin O.,Kachaeva M.,Kobzar O.,Keith K.A.,Harden E.A.,Hartline C.B.,James S.H.,Vovk A.,Brovarets V.. In Silico Design and Experimental Validation of Novel Oxazole Derivatives Against Varicella zoster virus. Molecular Biotechnology. 2023. Р. 1-11
25. Los O.V.,Sinenko V.O.,Kobzar O.L.,Zhirnov V.V.,Vovk A.I.,Brovarets V.S.. Synthesis and in vitro anticancer potential of new thiazole-containing derivatives of rhodanine. Chemistry of Heterocyclic Compounds. 2023. V. 59, N 6-7. Р. 484-493
26. Zhirnov V.,Shablykin O., Chumachenko S.,Kornii Y.,Keith K. A.,Harden E. A.,Hartline C.B.,James S.H.,Kobzar O.,Kovalishyn V.,Vovk A.Brovarets V.. In vitro activity of novel 4-iminohydantoin sulfamide derivatives against human cytomegalovirus. Chemical Papers. 2023. Р. 1-8
27. Hodyna D.,Kovalishyn V., Kachaeva M.,Shulha Y.,Klipkov A.,Shaitanova E.,Kobzar O.,Shablykin O.,Metelytsia L.. In Silico, In Vitro and In Vivo Study of Substituted Imidazolidinone Sulfonamides as Antibacterial Agents. Chemistry & Biodiversity. 2023. Р. e202301267
28. Derevyanchuk M.Kretynin S., Bukhonska Y., Pokotylo I., Khripach V., Ruelland E., Filepova R., Dobrev P.I., Martinec, J., Kravets V.. Influence of Exogenous 24-Epicasterone on the Hormonal Status of Soybean. Plants. 2023. V.12. N 20. Р. 3586
29. Kretynin S.V., Kolesnikov Y.S.. The role of calcium in implementation of the effect of brassinosteroids during the induction of oxidative stress in tobacco. Cytology and Genetics. 2023. V. 57. Р. 312-319
30. Rogalsky S., Tarasyuk O., Vashchuk A., Dzhuzha O., Cherniavska T., Makhno S.. Thermophysical properties and ionic conductivity of new imidazolium based protic ionic liquids. Journal of Molecular Liquids. 2023. V. 382. Р. 121942
31. Lishchuk P., Vashchuk A., Rogalsky S., Chepela L., Borovyi M., Lacroix D., Isaiev M.. Thermal transport properties of porous silicon filled by ionic liquid nanocomposite system. Scientific Reports. 2023. V.13. Р. 5889
32. Rogalsky S., Tarasyuk O., Babkina N., Makhno S., Pertko O., Povazhnyi V., Cherniavska T., Fatyeyeva K.. Fabrication of new proton conducting membrane for fuel cell applications based on porous polyimide Matrimid® and hydrophobic protic ionic liquid. Journal of Applied Polymer Science. 2023. V. 140, N 15. Р. e53731
33. Talaniuk V., Godzierz M., Vashchuk A., Iurhenko M., Chaber P., Sikorska W., Kobyliukh A., Demchenko V., Rogalsky S., Szeluga U., Adamus G.. Development of Polyhydroxybutyrate – Based Packaging Films and Methods to Their Ultrasonic. Materials. 2023. V.16, N 20. Р. 6617
34. Rogalsky S., Hodyna D., Semenyuta I., Frasinyuk M., Tarasyuk O., Riabov S., Kobrina L., Tetko I., Metelytsia L.. Antibacterial activity of 1-dodecylpyridinium tetrafluoroborate and its inclusion complex with sulfobutyl ether-b-cyclodextrin against MDR Acinetobacter baumannii strains. Innovative Biosystems and Bioengineering. 2023. V.7, N 4.Р. 25-35
35. Vortman M.Ya., Berezhnytska O.S., Aksenovska O.A., Kobylinskyi S.M., Kobrina L.V., Lemeshko V.N., Shevchenko V.V.. Guanidinium-containing oligoether as a complexing agent of transition metal ions. Functional Materials. 2023. V.30, N 1. Р. 120-127
36. Patrylak L.,Konovalov S.,Yakovenko A.,Pertko O.,Povazhnyi V.. Polycationic Nanostructured Faujasite Zeolite Catalysts for Glucose Transformation into 5-Hydroxymethylfurfural. Applied Nanoscience. 2023,V. 13. Р. 5743–5754https://doi.org/10.1007/s13204-023-02820-7
37. Shvets O.V.,Kurmach M.M., Yaremov P.S., Voloshyna Yu.G., Shcherban N.D.. Zeolite nanocomposites with variable acid and basic properties: effective catalysts for fine chemical synthesis and industrial reaction. Applied Nanoscience. 2023. https://doi.org/10.1007/s13204-023-02955-7
38. Muzychka L.,Boiko I.,Vrynchanu N., Smolii O.. Synthesis, antibacterial, and antibiofilm activities of pulmonarin B analogues. Curr. Chem. Lett. 2024. V. 24. doi:10.5267/j.ccl.2023.11.005
39. I. Semenyuta, D. Hodyna, V. Kovalishyn, B. Demydchuk, M. Kachaeva,S. Pilyo, V. Brovarets, L. Metelytsia. Development and application of in silico models to design new antibacterial5-amino-4-cyano-1,3-oxazoles against colistin-resistant E. coli strains. Artificial Intelligence Chemistry. 2023. V. 1, N 2. Р. 100024.https://doi.org/10.1016/j.aichem.2023.100024
40. D. Hodyna, V. Kovalishyn, Y. Romanenko, I. Semenyuta,V. Blagodatny, M. Kachaeva, O. Brazhko L. Metelytsia. Quinoline Hydrazone Derivatives as New Antibacterialsagainst Multidrug Resistant Strains. Chem. Biodiversity 2023. V. 20, N 10. Р. e202300839doi.org/10.1002/cbdv.2023008
41. D. Hodyna,V. Kovalishyn,I. Semenyuta,M. Kachaeva,Y. Shulha,M. Bugera, V. Blagodatny, O. Shablykin,L. Metelytsia. Design and Biological Evaluation of 4-Iminohydantoin Sulfamides as New Anti-Acinetobacter baumannii Agents. Biointerface Res. Appl. Chem. 2023. V. 13, N 6. P. 511-524.DOI: https://doi.org/1.33263/BRIAC136.511
42. G. Mrug,D. Hodyna,L. Metelytsia,V. Kovalishyn,O. Trokhimenko, S. Bondarenko,K. Kondratyuk,A. Kozitskiy, M. Frasinyuk. Structure-Activity Relationship Prediction-Based Synthesis and Cytotoxicity Evaluation against the HEp-2 Laryngeal Carcinoma Cell of Isoflavone–Cytisine Mannich Bases. Chemistry & Biodiversity. 2023. V. 20, N 8. Р. e202300560.https://doi.org/10.1002/cbdv.202300560
43. Pilyo S.G., Demydchuk B.A., Moskvina V.S., Shablykina O.V., Brovarets V.S.. A combinatorial library of substituted 3-sulfonyl-2-imino-1,2-dihydro-5H-dipyrido[1,2-a:2′,3′-d]pyrimidin-5-ones and their anticancer activities. Biopolym. Cell. 2022. V. 38, N 4. Р. 242-256. http://dx.doi.org/10.7124/bc.000A7B
44. Nizhenkovska I.V., Matskevych K.V., Golovchenko O.I., Golovchenko O.V., Kustovska A.D., Van M.. New prospective phosphodiesterase inhibitors: phosphorylated oxazole derivatives in treatment of hypertension. Adv. Pharm. Bull. 2023. V.13, N 2. С. 399-407. https://doi.org/10.34172/apb.2023.044
45. Zyabrev V., Demydchuk B., Zhirnov V., Brovarets V.. Synthesis, characterization, and in vitro anticancer evaluation of 2-aryl-4-arylsulfonyl-5-RS-1,3-oxazoles. Biointerface Res. Appl. Chem. 2023. V.13, N 3. P. 300. DOI: 10.33263/BRIAC133.300
46. Kovalishyn V., Severin O., Kachaeva M., Semenyuta I., Keith K.A., Harden E.A., Hartline C.B., James S.H., Metelytsia L., Brovarets V.. Design and experimental validation of the oxazole and thiazole derivatives as potential antivirals against of human cytomegalovirus. SAR and QSAR in Environmental Res. 2023. V.34, N 7. P. 523-541
47. Bondar D., Bragina O., Lee Ji Y., Semenyuta I., Jӓrving I., Brovarets V., Wipf P., Bahar I., Karpichev Y.. Hydroxamic Acids as PARP-1 Inhibitors: Molecular Design and Anticancer Activity of Novel Phenanthridinones. Helv. Chim. Acta. 2023. https://doi.org/10.1002/hlca.202300133
48. Zyabrev V., Pilyo S., Demydchuk B., Kachaeva M., Semenyuta I., Zhirnov V., Velihina Ye., Brovarets V.. Synthesis, characterization and in vitro anticancer evaluation of 5-sulfinyl(sulfonyl)-4-arylsulfonyl substituted 1,3-thiazoles. Chem. Med. Chem. 2023. V.18, N 14. Р. E202300161
49. Shablykin O.V., Merzhievskyi D.O., Brovarets V.S., Shishkina S.V.. New oxazole to oxazole recyclization. Chem. Het. Compd. 2023. V. 59, N 6. P. 521-524
50. Konovalenko A.S., Shablykin O.V., Shablykina O.V., Moskvina V.S., Shishkina S.V., Kozytskyi A.V., Brovarets V.S.. Distinctive features of 3-acetyl- and 3-benzoylisocoumarins’ interaction with active primery amines. Chem. Select. 2023. V.8, N 37. Р. e202301380. https://doi.org/10.1002/slct.202301380
51. Golovchenko O.V., Brusnakov M.V., Shabelko Yu.O., Brovarets V.S., Vydzhak R.M., Bahrieieva O.S., Potikha L.M., Shishkina S.V.. Synthesis and properties of methanesulfonyl derivatives of diethyl esters of 5-(hydroxyalkylamino)-1,3-oxazol-4-yl-phosphonic acids. Phosphorus, Sulfur, and Silicon and the Related Elements. 2023. DOI: 10.1080/10426507.2023.2251639
52. Shaydyuk Ye.O., Bashmacova N.V., Klishevich G.V., Dmytruk A.M., Kachkovsky O.D., Kuziv Ya.B., Dubey I.Ya., Befield K.D., Bondar M.V.. Nature of linear spectra; properties and fast relaxations in the excited states and two-photon absorption efficiency of 3-thiazolyl and 3-phenylthiazolyl coumarin derivatives.. ACS Publications. 2023. V.18, N 12. P. 11564-11573
53. Brusnakov M.Yu., Golovchenko O.V., Potikha L.M., Brovarets V.S.. Condenced azole-based organophosphorus heterocycles. Chem. Het. Compd. 2023. V.59, N 4/5. P. 217-236. Doi:10.1007/s10593-023-03184-0
54. Konovalenko A., Shablykin O., Shablykina O., Kozytskyi A., Brovares V.. Convenient and versatile method of 8-amino-6-(2-R-thiazol-4-yl)1,7-naphthyridines. Curr. Chem. Lett. 2024. V.13, N 1. P. 163-172. Doi: 10.5267/j.ccl.2023.7.004
55. Nallaparaju J.V., Nikonovich T., Jarg T., Merzhyievskyi D., Aav R., Kananovich D.G.. Mechanochemistry – amended barbier reaction as an expedient alternative to Grignar synthesis. Angew. Chem. Int. Edd. 2023. E202305775.
56. Dibchak D., Snisarenko M., Mishuk A., Shablykin O., Bortnichuk L., Klymenko-Ulianov O., Kheylik Yu., Sadkova I., Rzepa H.S., Mykhailiuk P.K.. General synthesis of 3‐azabicyclo [3.1.1]heptanes and evaluation of their properties as saturated isosteres. Angewandte Chemie. 2023. V.135, N 39. Р. e202304246. https://doi.org/10.1002/ange.202304246
57. Kirichok A.,Tkachuk H., Kozyriev Ye., Shablykin O., Datsenko O., Granat D., Yegorova T., Bas Yu., Semirenko V., Pishel I., Kubyshkin V., Lesyk D., Klymenko-Ulianov O., Mykhailiuk P.K.. 1‐Azaspiro[3.3]heptane as a bioisostere of piperidine. Angewandte Chemie. 2023. e202311583. https://doi.org/10.1002/ange.202311583
58. Krasylov I.V., Moskvina V.S., Khilya V.P.. Unexpected but prominent imines formation in Beckmann rearrangement of (spiro)pyranocoumarin oximes. Tetrahedron Lett. 2023. V. 129. P. 154747. https://doi.org/10.1016/j.tetlet.2023.154747
59. Tsygankova V.A., Voloshchuk I.V., Andrusevich Ya.V., Kopich V.M., Pilyo S.G., Klyuchko S. V., Brovarets V.S.. Use of pyridine and pyrimidine derivatives as new wheat growth regulators. Global Meet on Food Science and Technology”. March 23, 2023. Webinar GMFST 2023, LAS VEGAS, USA. P. 19-20
60. Chernykh A.V., Kudryk O.V., Olifir O.S., Dobrydnev A.V., Rusanov E., Moskvina V.S., Volochnyuk D.M., Grygorenko O.O.. Expanding the chemical space of 1,2-difunctionalized cyclobutanes. J. Org. Chem. 2023. V. 88, N 5. P. 3109-3131. https://doi.org/10.1021/acs.joc.2c02892
61. Chen X., Lv X., Gao L., Liu J., Wang W., Guo L., Frasinyuk M. S., Zhang W., Watt D. S., Liu C., Liu X.. Chalcone derivative CX258 suppresses colorectal cancer via inhibiting the TOP2A/Wnt/β-Catenin signaling. Cells. 2023. V.12, N 7. P. 1066. https://doi.org/10.3390/cells12071066
62. Myshko A., Mrug G., Kondratyuk K., Demydchuk B., Bondarenko S., Frasinyuk M.. An expedient synthesis of functionalized pyrazole-based aurone analogs.. Chemistry Select. 2023. V.8, N 20. Р. e202300257. https://doi.org/10.1002/slct.202300257
63. Myshko N.V., Mrug G.P., Kondratyuk K.M., Bondarenko S.P., Frasinyuk M.S.. Coumarin-based homoisoflavonoids as precursors in the synthesis of 8-heteroarylmethylcoumarins. Chem. Heterocycl. Compd. 2023. V. 59, N 6/7. P. 456-464. https://doi.org/10.1007/s10593-023-03216-9
64. Levterov V., Panasyuk Ya., Sahun K., Stashkevich O., Badlo V., Shablykin O., Sadkova I., Bortnichuk L., Klymenko-Ulianov O., Holota Yu., Lachmann L., Borysko P., Horbatok K., Bodenchuk I., Bas Yu., Dudenko D., Mykhailiuk P.K.. 2-Oxabicyclo [2.2.2]octane as a new bioisostere of the phenyl ring. Nature Commun. 2023. V.14, N 1. P. 5608. https://doi.org/10.1038/s41467-023-41298-3
65. Goulden T., Bodachivskyi Iu., Padula M.P., Williams D.B.G.. Concentrated ionic liquids for proteomics: Caveat emptor. International Journal of Biological Macromolecules. 2023. V. 253, № 7. Р. 127438. https://doi.org/10.1016/j.ijbiomac.2023.127438.
66. Kornii Yu., Shablykin O., Tarasiuk T., Stepaniuk O., Matvienko V., Aloshyn D., Zahorodniuk N., Sadkova I.V., Mykhailiuk P.K.. Fluorinatedaliphatic diazirines: preparation, characterization, and model photolabeling studies. J. Org. Chem. 2023. V. 88, N 1. P. 1-17. Doi:10.1021/acs.joc.2c02262
67. Malets Ye. S., Vashchenko B. V., Moskvina V.S., Golovchenko O.V., Brovarets V.S., Grygorenko O.O.. Parent 5(7)-azachromones and their partially hydrogenated derivatives: synthesis and physiochemical properties. Chem. Heterocycl. Comp. 2023. V.59, N 6/7. P. 494-499
68. Kukushkina K.V., Moskvina V.S., Shablykina O.V., Khilya V.P.. Expanding the isoflavone, pyrazole, and oxazole chemical space through 2′-carboxamido-2-hydroxy-deoxybenzoin precursors.. Chem. Heterocycl. Comp. 2023. V.59, N 6/7. P. 479-483. https://doi.org/10.1007/s10593-023-03219-6
69. Lyutenko N.V., Sorochinsky A.E., Soloshonok V.A.. Asymmetric synthesis of pyroglutamic acids via Ni(II) complex methodology. Chem. Heterocycl. Comp. 2023. Р. 332-340. https://doi.org/10.1007/s10593-023-03203-0
70. Shablykin O.V., Brovarets V.S., Shablykina O.V.. Recyclization of 5-aminooxazoles as a route to new functionalized heterocycles (developments of V.P. Kukhar institute of bioorganic chemistry and petrochemistry of the NAS of Ukraine). Chem. Record. 2023. e202300264. https://doi.org/10.1002/tcr.202300264
71. Gaponov A.M., Pavlenko O.L., Dmytrenko O.P., Kulish M.P., Ryzhkova A.S., Lesiuk A.I., Obernikhina N.V., Łuszczyńska B., Kachkovsky O.D.. Molecular heteroassociation in films of thiochrome and tryptophan. Mol. Cryst. Liquid Cryst. 2023. https://doi.org/10.1080/15421406.2023.2257515
72. Tsygankova V.A., Andrusevich Ya.V., Pilyo S.G., Brovarets V.S.. Effect of plant growth regulators and fertilizers of the vegetative growth of sunflowers (Helianthus annuus L). The scientific heritage. 2023.N 116. P. 3-9. DOI: 10.5281/zenodo.8129039
73. Tsygankova V.A., Andreev A.M., Andrusevich Ya.V., Pilyo S.G., Klyuchko S.V., Brovarets V.S.. Use of synthetic plant growth regulators in combination with fertilizers to improve wheat growth. Int J Med Biotechnol Genetics. 2023. S1:02:002:9-14. URL: http://scidoc.org/IJMBGS1V2.php
74. Tsygankova V.A., Voloshchuk I.V., Kopich V.M., Pilyo S.G., Klyuchko S.V., Brovarets V.S.. Studying the effect of plant growth regulators Ivin, Methyur and Kamethur on growth and productivity of sunflower. J. Advanc. Agricult. 2023. V.14. P. 17-24. DOI: https://doi.org/10.24297/jaa.v14i.9453
75. Tsygankova V.A., Andrusevich Ya.V., Kopich V.M., Voloshchuk I.V., Pilyo S.G., Klyuchko S.V., Brovarets V.S.. Application of pyrimidine and pyridine derivatives for regulation of chickpea (Cicer arietinum L.) growth. Int. J. Innovat. Sci. Res. Techn. (IJISRT). 2023. V.8, N 6. P. 19-28. DOI: https://doi.org/10.5281/zenodo.8020671
76. Tsygankova V.A., Kopich V.M., Voloshchuk I.V., Pilyo S.G., Klyuchko S.V., Brovarets V.S.. New growth regulators of barley based on pyrimidine and pyridine derivatives. Sciences of Europe. 2023. N. 124. P. 13-23. https://doi.org/10.5281/zenodo.8327852.
77. Tsygankova V.A., Andrusevich Ya.V., Kopich V.M., Voloshchuk I.V., Bondarenko O.M., Pilyo S.G., Klyuchko S.V., Brovarets V.S.. Effect of pyrimidine and pyridine derivatives on the growth and photosynthesis of pea microgreens. Int. J. Med. Biotechnol. Genetics. 2023. S1:02:003:15-22. https://UBAscidoc.org/IJMBGS1V2.php
78. Tsygankova V.A., Andreev A.M., Andrusevich Ya.V., Kopich V.M., Klyuchko S.V., Pilyo S.G., Brovarets V.S.. Use of Ivin, Methyur, Kamethur and microfertilizers to improve the growth of oilseed flax (Linum usitatissimum L.). Annali d’Italia. 2023. N. 48. P. 3-10. https://doi.org/10.5281/zenodo.10034698.
79. Hodyna D.M., Kovalishyn V.V., Derevianko K.Yu., Pilyo S.G., Metelytsia L.O.. 1,3-Oxazole derivatives as antibacterials against colistin-resistants acinetobacter baumanni strains. IV Intern. Scient. Theoret. Conf. 16 june 2023. Athens: Hellenic Rep. P. 83-85
80. Semenyuta I.V., Hodyna D.M., Kovalishyn V.V., Demydchuk B. A., Pilyo S.G., Metelytsia L.O.. 5-Amino-4-cyano-1,3-oxazoles as new antibacterials against antibiotic-resistants Escherichia coli strains. IV Intern. Scient. Practical. Conf. 16 may 2023. Boston: USA. P. 117-121
81. Tsygankova V.A., Andreev A.M., Andrusevich Ya.V., Kopich V.M., Pilyo S.G., Klyuchko S.V., Brovarets V.S.. Synergistic effect of synthetic plant growth regulators and microfertilizers on the growth of canola (Brassica napus L.). Danish Scient. J. (DSJ). 2023. V.1, N. 77. P. 8-12. https://doi.org/10.5281/zenodo.10053315
82. Tsygankova V.A., Voloshchuk I.V., Andrusevich Ya.V., Kopich V.M., Oliynyk O.O., Stefanovska T.R., Pidlisnyuk V., Pilyo S.G., Klyuchko S.V., Brovarets V.S.. Use of synthetic plant growth regulators in agriculture and biotechnology.. Polish J. Sci. 2023. V. 1, N. 68. P. 12-17. https://doi.org/10.5281/zenodo.10131991.
83. Bondar M.V., Faryadras S., Munera N., Chang H.-T., Uddin M., Beldield K.D., Kachkovsky O.D., Van Stryland E.W., Hagan D.J.. New two-photon absorbing Squaraine derivative with efficient near-infrared fluorescence, superluminescence, and high photostability. J. Phys. Chem. B. 2022. V.126, N 21. P. 3897-3907
84. Severin O.O., Kachaeva M.V., Pilyo S.G., Kovalishyn V.V., Keith K.A., Harden E.A., Hartline C.B., James S.H., Zhirnov V.V., Brovarets V.S.. Synthesis, characte­ri­za­tion and study of anti-HPV activity and cell cytotoxicity of novel 1,3-oxazole-4-carbonitrile and 4-sulfonylamide-5-phenyl-1,3-thiazole derivatives in vitro. Letters in Applied Nanobioscience. 2023. https://doi.org/10.33263/LIANBS120.000
85. Denisenko A., Garbuz P., Makovetska Ye., Shablykin O., Lesyk D., Al-Maali G., Korzh R., Sadkova I., Mykhailiuk P.. 1,2-Disubstituted bicyclo[2.1.1]hexanes as bioisosteres of the ortho-substituted benzene. Chem. Sci. 2023. 10.1039/D3SC05121H
86. E. Shaitanova, V. Matoušek, T. Herentin, M. Adamec, R. Matyáš, B. Klepetářová, P. Beier. Synthesis and Cycloaddition Reactions of 1-Azido-1,1,2,2-tetrafluoroethane. J. Org. Chem. 2023. V. 88, N 21. Р. 14969-14977
87. J. He, Z. Li, G. Dhawan, W. Zhang, A. E. Sorochinsky, G. Butler, V. A. Soloshonok, J. Han. Fluorine-containing drugs approved by the FDA in 2021. Chinese Chemical Letters. 2023. V. 34. Р. 107578
88. N.V. Lyutenko, A.E. Sorochinsky, V.A. Soloshonok. Asymmetric synthesis of pyroglutamic acids via Ni(II)-complex methodology. Chemistry of Heterocyclic Compounds. 2023. V. 59. Р. 332-340
89. Romanenko V.D.. Synthetic strategies toward and around the CF3S(O) structural motif. Current Organic Chemistry. 2023. V. 27. Р.411-434.DOI: 10.2174/1385272827666230517114921
90. Holovach S.,Melnykov K.P.,Poroshyn I.,Iminov R.T.,Dudenko D.,Kondratov I.S.,Levin M.,Grygorenko O.O.. C−C Coupling through Nitrogen Deletion: Application to Library Synthesis. Chemistry A European Journal. 2023. V. 29, N 4.Р. e202203470https://doi.org/10.1002/chem.202203470
91. Fink E. A., Bardine C.,Gahbauer S., Singh I.Detomasi T. C.,White K., Gu S.,Wan X., Chen J.,Ary B., Glenn I.,O’Connell J.,O’Donnell H.,Fajtov P., Lyu J.,Vigneron S.,Young N.J.,Kondratov I.S.,Alisoltani A.,Simons L.M.,Lorenzo-Redondo R.,Ozer E. A.,Hultquist J.F.,O’Donoghue A. J.,Moroz Y.S.,Taunton J.,Renslo A.R.,Irwin J.J.,García-Sastre A.,Shoichet B.K.,Craik C.S.. Large library docking for novel SARS‐CoV‐2 main protease non‐covalent and covalent inhibitors. Protein Science. 2023. V. 32. Р. e4712https://doi.org/10.1002/pro.4712
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93. Rud A.D., Kornienko N.E., Polunkin I.V., Boguslavskii L.Z., Vinnichenko D.V., Kirian I.M., Kolomys O.F., Kuskova N.I.. Structure of carbon nanospheres modified with oxygen-containing groups and halogens. Applied Nanoscience. 2023. № 10. Р. 6929-6937. DOI: https://doi.org/10.1007/s13204-023-02817-2

2022 р.

Розділи в зарубіжних монографіях

• V.A. Tsygankova, Ya.V. Andrusevich, O.I. Shtompel, R.M. Solomyanny, A.O. Hurenko, M.S. Frasinyuk, G.P. Mrug, O.V. Shablykin, S.G. Pilyo, A.M. Kornienko, V.S. Brovarets. New Auxin and Cytokinin Related Compounds Based on Synthetic Low Molecular Weight Heterocycles. Auxins, Cytokinins and Gibberellins Signaling in Plants. Signaling and Communication in Plants. Aftab, T. (Eds). Springer Nature. Switzerland AG. 2022. 377 p. Pp. 353-377.

• S. Konovalov,S. Zubenko,L. Patrylak, A. Yakovenko, V. Povazhnyi, K. Burlachenko. Revisiting the Synthesis of Fatty Acid Alkyl Esters of Lower Monohydric Alcohols by Homogeneous Base-Catalyzed Transesterification of Vegetable Oils. Chemmotological Aspects of Sustainable Development of Transport. Sustainable Aviation. 2022, Springer, Cham.Р. 49-80 https://doi.org/10.1007/978-3-031-06577-4_4

Публікації в зарубіжних виданнях

1. D. Hodyna, V. Kovalishyn, I. Semenyuta, S. Rogalsky, O. Trokhimenko, A. Gryniukova, L. Metelytsia. Ester-Functionalized Imidazolium- and Pyridinium-Based Ionic Liquids: Design, Synthesis and Cytotoxicity Evaluation. Biointerface Research in Applied Chemistry. 2022. V. 12, N 3. P. 2905-2957. doi.org/10.33263/BRIAC123.29052957
2. L.O. Metelytsia,D.M. Hodyna, I.V. Semenyuta,V.V. Kovalishyn,S.P. RogalskyY.K. Derevianko, V.S. Brovarets,I.V. Tetko. Theoretical and Experimental Studies of Phosphonium Ionic Liquids as Potential Antibacterials of MDR Acinetobacter baumannii. Journal of Antibiotics. 2022. V. 11. P. 491. https://doi.org/10.3390/antibiotics11040491.
3. Vydzhak R.N., Panchishin S.Y.,Kachaeva M.V.,Pilyo S.G., Moskvina V.S., Shablykina O.V., Kozytskiy A.V.,Brovarets V.S. Rapid synthetic approaches to libraries of diversified 1,2-dihydrochromeno[2,3-c]pyrrole-3,9-diones and 3-(2-hydroxyphenyl)-4,5-dihydropyrrolo[3,4-c]pyrazol-6(1H)-ones. Molecular diversity. 2022. Vol. 26, N 2. Р. 1115-1128.DOI: 10.1007/s11030-021-10234-2
4. O.V. Moshynets,T.P. Baranovskyi,O.S. Iungin, N.P. Kysil, L.O. Metelytsia,I. Pokholenko, V.V. Potochilova,G. Potters, K.L. Rudnieva,S.Y. Rymar, I.V. Semenyuta, A.J. Spiers, O.P. Tarasyuk,S.P. Rogalsky eDNA inactivation and biofilm inhibition by the polymeric biocide polyhexamethylene guanidine hydrochloride (PHMG-Cl). International Journal of Molecular Sciences. 2022. V. 23. Р. 731.DOI: 10.3390/ijms23020731.
5. Obernikhina N.V.,Kachaeva M.V., Kachkovsky O.D.,Brovarets V.S. In silico Study of Conjugated Nitrogen Heterocycles Affinity in their Biological Complexes Chemistry of Heterocyclic Compounds 2022. V. 58, N 8. Р. 412-420.DOI 10.1007/s10593-022-03107-5
6. D.S. Kamenskyh, T.V. Tkachenko, V.A. Yevdokymenko, Y.V. Sheludko, M.M. Filonenko, V.A. Povazhny, M.M. Baran, O.V. Pavluik, V.I. Kashkovsky Synthesis, characterization and optimization of the aluminum–nickel–molybdenum catalyst for hydrogenation Applied Nanoscience. 2022. P. 1-13. https://doi.org/10.1007/s13204-022-02644-x
7. T.V. Tkachenko, M.M. Baran, V.O. Yevdokymenko, D.S. Kamenskyh, V.I. Kashkovsky Optimization of Ether Production by Proton Current Materials Today: Proceedings. 2022. V. 62, N 15. P. 7643-7649. https://doi.org/10.1016/j.matpr.2022.02.004
8. L.K. Patrylak, S.V. Konovalov, A.V. Yakovenko, O.P. Pertko, V.A. Povazhnyi, Yu.G. Voloshyna, O.V. Melnychuk, M.M. Filonenko Micro–mesoporous kaolin-based zeolites as catalysts for glucose transformation into 5-hydroxymethylfurfural Applied Nanoscience. 2022. P.1-14. https://doi.org/10.1007/s13204-022-02620-5
9. L. Patrylak, S. Zubenko, S. Konovalov, A. Yakovenko, V. Povazhnyi, O. Pertko, Y. Voloshyna, O. Melnychuk Mykhailo Filonenko Іsomerization of limonene on zeolite-containing catalysts based on Кaolin Chemistry Journal of Moldova. 2022. P. 1857-1727. DOI: dx.doi.org/10.19261/cjm.2022.980
10. V. Pidlisnyuk, A. Mamirova, R.A. Newton, T. Stefanovska, O. Zhukov, V. Tsygankova, P. Shapoval The role of plant growth regulators in Miscanthus × giganteus utilisation on soils contaminated with trace elements Agronomy. 2022. V. 12, N 12. Р. 2999. https://doi.org/10.3390/agronomy12122999
11. Vasetska O., Zhminko P., Prodanchuk M., Galkin A., Tsygankova V. Perspective for using2,6-dimethylpyridine-N-oxide to reduce the toxic effect of xenobiotics in mammals J. Adv. Pharm. Educ. Res. 2022. V. 12, N 1. P. 21 – 29.
12. Tsygankova V.A., Voloshchuk I.V., Klyuchko S.V., Pilyo S.G., Brovarets V.S., Kovalenko O.A. The effect of pyrimidine and pyridine derivatives on the growth and productivity of sorghum International Journal of Botany Studies. 2022. V. 7, N 5. P. 19-31.https://www.botanyjournals.com/archives/2022/vol7/issue5/7-4-28
13. Tsygankova V.A., Voloshchuk I.V., Andrusevich Ya.V., Kopich V.M., Pilyo S.G., Klyuchko S.V., Kachaeva M.V., Brovarets V.S. Pyrimidine derivatives as analogues of plant hormones for intensification of wheat growth during the vegetation period Journal of Advances in Biology. 2022. V. 15. P. 1-10. DOI: https://doi.org/10.24297/jab.v15i.9237
14. Tsygankova V.A., Oliynyk O.O., Kvasko O.Yu., Pilyo S.G., Klyuchko S.V., Brovarets V.S. Effect of Plant Growth Regulators Ivin, Methyur and Kamethur on the Organogenesis of Miniature Rose (Rosa mini L.) in Vitro Int. J. Med. Biotechnol. Genetics. 2022. S1: V. 2, N 1. P.1-8.https://scidoc.org/IJMBG-2379-1020-S1-02-001.php
15. Y. Kolesnikov, S. Kretynin, Y. Bukhonska, I. Pokotylo, E. Ruelland, J. Martinec, V. Kravets Phosphatidic Acid in Plant Hormonal Signaling: From Target Proteins to Membrane Conformations Int. J. Mol. Sci. 2022, V. 23, N 6. Р. 3227; https://doi.org/10.3390/ijms23063227
16. Kobzar O.,Shulha Yu.,Buldenko V.,Cherenok S.,Silenko O.,Kalchenko V.,Vovk A. Inhibition of glutathione S-transferases by photoactive calix[4]arene α-ketophosphonic acids Bioorganic and Medicinal Chemistry Letters. 2022. V. 77. Р. 129019
17. Silenko O.,Cherenok S.,Shulha Yu.,Kobzar O.,Rusanov E.,Karpichev E.,Vovk A.Kalchenko V. Thiacalix [4] arene phosphoric acids. Synthesis, structure, and inhibition of glutathione S-transferases Phosphorus, Sulfur, and Silicon and the Related Elements. 2022. V.197 (5-6). Р. 538-541
18. Velihina Y.,Pilʹo S.,Kobzar O.,Zaliavska O.,Prichard M. N.,James S. H.Keith K.,Hartline C.,Zhirnov V.,Vovk A.,Brovarets V. Synthesis of some oxazolo [4, 5-d] pyrimidine derivatives and evaluation of their antiviral activity and cytotoxicity Arkivok. 2022. Р. 108-117
19. Obernikhina N.V., Kobzar O.L.,Kachaeva M.V., Kachkovsky O.D. , Brovarets V.S. In silico and in vitro estimation of structure and biological affinity of 1, 3-oxazoles: fragment-to-fragment approach Curr. Comput.-Aided Drug Des. 2022. V. 18. P. 95-109
20. Ivanenko I.,Ruda A.,Povazhnyi V. Cobalt-nitrogen-doped activated carbons for hydrogen generation Materials Today: Proceedings.2022. V. 62 ( P15). Р. 7691-7697
21. Yu.G. Voloshyna,O.P. Pertko,V.A. Povazhnyi,L.K. Patrylak Peculiarities of products’ distribution in n-hexane hydroisomerization on modified mordenite-containing rock Appl. Nanosci. 2022.https://doi.org/10.1007/s13204-022-02632-1
22. Yu. Kholodko, A. Bondarieva, V. Tobilko, V. Pavlenko, O. Melnychuk, V. Glukhovskyi Synthesis and characterization of kaolinite-based granular adsorbents for the removal of Cu(II), Cd(II), Co(II), Zn(II), and Cr(VI) from contaminated water Eastern-European Journal of Enterprise Technologies.2022. V. 4 N. 10. Р. 118
23. Rogalsky S., Tarasyuk O., Vashchuk A., Davydenko V., Dzhuzha O., Motrunich S., Cherniavska T., Papeikin O., Bodachivska L., Bardeau J.-F. Synthesis and evaluation of N,N-dibutylundecenamide as new eco-friendly plasticizer for polyvinyl chloride Journal of Materials Science. 2022. V. 57. Р. 6102-6114
24. Rogalsky S., Tarasyuk O., Dzhuzha O., Hodyna D., Cherniavska T., Hubina A., Filonenko M., Metelytsia L. Evaluation of N,N-dibutylolelamide as a bifunctional additive for poly(vinyl chloride) Colloid and Polymer Science. 2022. V. 300 (12). Р. 1-8
25. S.I. Vdovenko,I.I. Gerus,M. Pagacz-Kostrzewa,M. Wierzejewska Influence of the features of the spatial and electronic structure of α-substituted β-ethoxyvinyl trifluoromethyl ketones and secondary amines on their reactivity Journal of Molecular Structure. 2022. V. 1255. Р. 132417
26. J. Liu, W. Lin,A.E. Sorochinsky,G. Butler,A. Landa, J. Han,V.A. Soloshonok Successful trifluoromethoxy-containing pharmaceuticals and agrochemicals Journal of Fluorine Chemistry. 2022. V. 257-258. Р. 109978
27. J. Han,J. Escorihuela,S. Fustero,A. Landa,V.A. Soloshonok,A. Sorochinsky Asymmetric Michael addition in synthesis of β-substituted GABA derivatives Molecules. 2022. V. 27. Р. 3797
28. Q. Wang, J. Han, A. Sorochinsky, A. Landa, G. Butler, V. A. Soloshonok The latest FDA-approved pharmaceuticals containing fragments of tailor-made amino acids and fluorine Pharmaceuticals. 2022. V. 15. Р. 999
29. V.D. Romanenko From elusive monomeric metaphosphates to oligomeric metaphosphate reagents:New avenue to halogen-free phosphorylation of biomolecules Current Organic Chemistry. 2022. V. 26, Р. 432-437.DOI: 10.2174/1385272826666220330111824
30. Chernykh A.V.,Aloshyn D.,Kuchkovska Yu.O.,Daniliuc C.G.,Tolmachova N.A.,Kondratov I.S.,Zozulya S.,Grygorenko O.O., Haufe G. Impact of β-perfluoroalkyl substitution of proline on the proteolytic stability of its peptide derivatives Org. Biomol. Chem. 2022. V. 20. Р. 9337-9350. https://doi.org/10.1039/D2OB01430K
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33. Kondratov I.S.,Moroz Yu.S.,Irwin J.J.,Shoichet B.K. Drug building blocks and libraries at risk in Ukraine Science. 2022. V. 376(6596). Р. 929https://doi.org/10.1126/science.abq7841
34. Kondratov I.S.,Moroz Yu.S.,Grygorenko O.O.,Tolmachev A.A. The Ukrainian Factor in Early-Stage Drug Discovery in the Context of Russian Invasion: The Case of Enamine Ltd ACS Med. Chem. Lett. 2022. V. 13. N 7. Р. 992-996. https://doi.org/10.1021/acsmedchemlett.2c00211
35. M. Aksylenko, E. Sheludko, N. Himach, V. Yevdokimenko Polygalacturonates of biogenic metals – prospective components of new composite preparations for wheat J. Annual Research & Review in Biology. 2022. V. 37 (12). P. 17-28 https://doi.org/10.9734/arrb/2022/v37i1294273
36. A.O. Kolodiazhna,O.I. Kolodiazhnyi Сatalytic asymmetric synthesis of C-chiral phosphonate Symmetry. 2022. V. 14. P. 1758-1825https://doi.org/10.3390/sym14091758
37. D. Prysiazhnuk, A. Kolodiazhna, O. Kolodiazhnyi Сonvergent method for the determination of halo-2,3-dihydro-1H-inden-1-ol absolute configuration Arkivoc. 2022. V. IX. P. 23-32.https://doi.org/10.24820/ark.5550190.p011.835
38. N.A. Ogurtsov,A.V. Mamykin,O.L. Kukla,A.S. Pavluchenko,M.V. Borysenko,Yu.P. Piryatinski,J.-L. Wojkiewicz,A.A. Pud The impact of interfacial interactions on structural, electronic and sensing properties of poly(3-methylthiophene) in the core-shell nanocomposites. Application to the CWA simulants detection Macromolecular Materials and Engineering. 2022. V. 307(4). P. 2100762
39. T. Feng, Y. Yuan, X. Chen,S. Zhao, M. Cao, L. Feng,S. Shi, H. Wang,T. Liu, A. Pud,L. Han, R. Scaffaro, B. He, N. Wang Ultrasensitive and highly specific detection of iodine ions using zirconium (IV)-enhanced oxidation Cell Reports Physical Science. 2022. V. 3 (11). P. 101143 (10 pages)
40. Potikha L.M., Brovarets V.S., Zhirnov V.V. Anticancer evaluation of difunctional substituted 1,2-dihydrophthalazines Chem. Data Collect. 2022. V. 37. P. 100817. https://doi.org/10.1016/j.cdc.2021.100817
41. Demydchuk B.A., Mykhalchenko O.A., Rusanov E.B., Moskvina V.S., Brovarets V.S. Regioselective synthesis of 5H-imidazolo[1,2-e][1,3,5]triazepines Arkivoc. 2022. V. ІІ. P. 204-214
42. Nizhenkovska I.V., Matskevych K.V., Golovchenko O.I., Golovchenko O.V., Kustovska A.D., Van M. New prospective phosphodiesterase inhibitors: phosphorylated oxazole derivatives in treatment of hypertension Adv. Pharm. Bull., 2022. DOI: 10.34172/apb.2023.044
43. Brusnakov M., Golovchenko O., Velihina Ye., Liavynets O., Zhirnov V., Brovarets V. Evaluation of anticancer activity of 1,3-oxazol-4-ylphosphonium salts in vitro Chem. Med. Chem. 2022. V. 17, № 20. P. e202200319. DOI: 10.1002/cmdc.202200319
44. Biletska I.M., Mrug G.P., Prostota Ya.O., Kondratyuk K.M., Bondarenko S.P., Frasinyuk M.S. Synthesis of 2-trifluoroacetonyl-3-alkyl/alkoxy-chromones and their reactions with 1,2-bidentate nucleophiles Heterocycles. 2022. V. 104, N 7. P. 1229-1244
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49. Glibov E.K., Gorbulenko N.V., Moskvina V.S., Suprun A.V., Shablykina O.V. Shokol T.V., Khilya V.P. Synthesis and recyclization of methylenbisflavonoids based on heterocyclic analogues of umbelliferon and formononetin Chem. Nat. Compd. 2022. V. 58, N 4. P. 617-622. https://doi.org/10.1007/s10600-022-03755-1
50. Konovalenko A.S., Shablykina O.V., Shablykin O.V., Moskvina V.S., Brovarets V.S. 1H-isochromene-1-ones and isoquinoline-1(2H)-ones with carbonyl group in position 3: Features of synthetic approaches and transformation Arkivoc. 2022. V. VІІІ. P. 79-112. https://doi.org/10.24820/ark.5550190.p011.861
51. Potikha L.M., Brovarets V.S., Zhirnov V.V. Biological evaluation of 3-aminoisoquinolin-1(2H)-one derivatives as potential anticancer agents French-Ukr. J. Chem. 2021. V.9, №2. P. 52-63
52. A.V. Mamykin, O.L. Kukla, A.S. Pavluchenko, Z.I. Kazantseva, I.A. Koshets, A.A. Pud, N.A. Ogurtsov, Yu.V. Noskov, V.I. Kalchenko Electronic nose-type chemosensory systems for detection of gaseous poisonous substances Semiconductor Physics, Quantum Electronics & Optoelectronics. 2022. V.25, No.4. Р. 429-440https://doi.org/10.15407/spqeo25.04.429

2021 р.

Розділи в зарубіжних монографіях

1. V.D. Romanenko, J.-M. Sotiropoulos. Six-membered rings with two or more heteroatoms with at least one boron.Comprehensive Heterocyclic Chemistry IV, Elsevier. New York. 2021. Р.1-40. DOI: 10.1016/B978-0-12-818655-8.00098-6.
2. Yakovlieva A., Boichenko S., Zubenko S., Konovalov S. Synthesis and physico-chemical properties of palm kernel oil bioadditives for alternative jet fuel. Systems and means of motor transport. Seleced problems. Seria: Transport. Mono-grafia. Rzeszow (Poland). 2021. Р. 257-264.
3. Grygorenko O.O., Hutskalova V., Moskvina V.S. Bicyclic 6-6 system with one bridgehead (ring junction) nitrogen atom: three extra heteroatoms (2:1).Chapter in book: “Comprehensive heterocyclic chemistry IV (Fourth edition)”, 2022. P. 216-278. https://doi.org/10.1016/b978-0-12-409547-2.14958-3.
4. Tsygankova V.A.Characterisation of Endo-Polygalacturonases activities of Rice (Oryza sativa) Fungal Pathogens in Nigeria, West Africa.Chapter in book: Grain and Seed Proteins Functionality (Jimenez-Lopez, J.C. Ed). Chapter 10. 2021. Intechopen Limited, London, United Kingdom. DOI:10.5772/intechopen.94763.

Публікації в зарубіжних виданнях

1. I.G. Logvinenko, I.S. Kondratov, A.V. Dobrydnev, A.V. Kozytskiy, O.O. Grygorenko. Synthesis and reactions of ω-CF3O-substituted aliphatic sulfonyl chlorides.Journal of Fluorine Chemistry. 2021. V. 246. Р. 109799.
2. J. Han, N. Lyutenko, A. Sorochinsky, A. Okawara, H. Konno, S. White, V. Soloshonok. Tailor-Made Amino Acids in Pharmaceutical Industry: Synthetic Approaches to aza-tryptophane derivatives. Chem. Eur. J. 2021. doi.org/10.1002/chem.202102485
3. E.N. Shaitanova, O.A. Balabon, A.N. Rybakova, T.S. Khlebnicova, F.А. Lakhvich, I.I. Gerus. Synthesis of functionalized fluoroalkyl pyrimidines and pyrazoles from fluoroalkyl enones. Journal of Fluorine Chemistry. 2021. V. 252. Р. 109905 https://doi.org/10.1016/j.jfluchem.2021.109905
4. A.A. Homon, O.V. Hryshchuk, O.V. Mykhailenko, B.V. Vashchenko, K.P. Melnykov, O.M. Michurin, C.G. Daniliuc, I.I. Gerus, V.O. Kovtunenko, I.S. Kondratov, O.O. Grygorenko. 4-(Di‐/Trifluoromethyl)‐2‐heterabicyclo[2.1. 1]- hexanes: advanced fluorinated phenyl isosteres and proline analogues. European Journal of Organic Chemistry. 2021 https://doi.org/10.1002/ejoc.202100414
5. S. Trofymchuk, M. Bugera, A. Klipkov, V. Ahunovych, B. Razhyk, S. Semenov, A. Boretskyi, K. Tarasenko, P. Mykhailiuk. Scalable Approach to Fluorinated Heterocycles with Sulfur Tetrafluoride (SF4).J. Org. Chem. 2021. V. 86, № 17. Р. 12181-12198 https://doi.org/10.1021/acs.joc.1c01518
6. V.D. Romanenko. New trends in development of P-C bond forming reactions. Current Organic Chemistry. 2021. V.25, № 17. Р. 1937-1976 DOI: 10.2174/1385272825666210610153954
7. Noskov Yu., Ogurtsov N., Bliznyuk V., Lvov Yu., Myronyuk I., Pud A. Synthesis and properties of coreshell halloysite–polyaniline nanocomposites. Applied Nanoscience. 2021. https://doi.org/10.1007/s13204-021-01812-9
8. O.I. Kolodiazhnyi. Phosphorus Compounds of Natural Origin: Prebiotic, Stereochemistry, Application. Symmetry. 2021. V. 13(5)., № 889. Р. 1-52.
9. D.V. Prysiazhnuk, E.B. Rusanov, O.I. Kolodiazhnyi. The absolute configuration of 2-bromo-2,3-dihydro-1H-inden-1-ols. Synthetic communications. 2021. V. 51, № 19. Р. 3023–3031
10. O.O. Kolodiazhna, D.V. Prysiazhnuk, A.O. Kolodiazhna, O.I. Kolodiazhnyi. Synthesis of optically active vicinal fluorocyclopentanols and fluorocyclopentanamines by enzymatic deracemization. Arkivoc 2022, p. iii. Р. 14-26 https://doi.org/10.24820/ark.5550190.p011.634
11. O. Kolodiazhnyi, A. Kolodiazhna, E. Grishkun, D. Prysiazhnuk, O. Kolodiazhna, S. Sheiko. Achievements in developments of stereochemistry. Phosphorus, sulfur, and silicon and the related elements. 2021. https://doi.org/10.1080/10426507.2021.2011874
12. A. Kolodiazhna, D. Prysiazhnuk, O. Kolodiazhnyi. Asymmetric Electrophilic Reactions in Phosphorus Chemistry.Phosphorus, sulfur, and silicon and the related elements. 2021. V. 196. https://doi.org/10.1080/10426507.2021.1989687
13. A. Kolodiazhna, E. Grishkun, O. Kolodiazhnyi. Synthesis of chiral phosphonobenzaldehydes and phosphonotyrosine. Phosphorus, sulfur, and silicon and the related elements 2021, 196. https://doi.org/10.1080/10426507.2021.1989686
14. Metelytsia L., Hodyna D., Dobrodub I., Semenyuta I., Zavhorodnii M., Blagodatny V., Kovalishyn V., Brazhko O. Design of (quinolin-4-ylthio)carboxylic acids as new Escherichia coli DNA gyrase B inhibitors: machine learning studies, molecular docking, synthesis and biological testing. Comput. Biol. Chem. 2020. V. 24, № 85. Р. 107224 https://doi.org/10.1016/j.compbiolchem.2020.107224
15. Metelytsia L.O., Trush M.M., Kovalishyn V.V., Hodyna D.M., Kachaeva M.V., Brovaret V.S., Pilyo S.G., Sukhoveev V.V., Tsyhankov S.A., Blagodatnyi V.M., Semenyuta I.V. 1,3-Oxazole derivatives of cytisine as potential inhibitors of glutathione reductase of Candida spp.: QSAR modeling, docking analysis and experimental study of new anti-Candida agents.. Comput. Biol. Chem. 2021. V. 90. Р. 107407 https://doi.org/10.1016/j.compbiolchem. 2020.107407
16. Hodyna D., Kovalishyn V., Semenyuta I., Blagodatny V., Rogalsky S., Metelytsia L. In silico and in vitro Studies of Imidazolium Ionic Liquids as Effective Antibacterial Agents against Multidrug Resistant Escherichia coli Strains.. Current Bioactive Comp. 2021. V. 17, № 2. P. 130–144 https://doi.org/10.2174/1573407216999200422115655
17. Semenyuta I., Trush M., Kovalishyn V., Rogalsky S., Hodyna D., Karpov P., Xia Z., Tetko I., Metelytsia L. Structure-Activity Relationship Modeling and Experimental Validation of the Imidazolium and Pyridinium Based Ionic Liquids as Potential Antibacterials of MDR Acinetobacter Baumannii and Staphylococcus Aureus. Int. J. Mol. Sci. 2021. V.22. Р. 563-576. https://doi.org/10.3390/ijms22020563
18. T.Tkachenko, Ye.Sheludko, V.Yevdokymenko, D.Kamenskyh, N. Khimach, V. Povazhny, M. Filonenko, M. Aksylenko, V. Kashkovsky. Physico-chemical properties of flax microcrystalline cellulose. Applied Nanoscience (2021). https://doi.org/10.1007/s13204-021-01819-2
19. O. Pertko, Yu.Voloshyna, A. Kontsevoi, V.Trachevskyi. Ethylbenzene formation and its conversion towards coke in the side-chain methylation of toluene on a basic X zeolite. Journal of Porous Materials. 2021. V.28. P. 1713–1723 https://doi.org/10.1007/s10934-021-01119-8.
20. L.K. Patrylak, O.P. Pertko, V.A. Povazhnyi, A.V. Yakovenko, S.V. Konovalov. Evaluation of nickel-containing zeolites in the catalytic transformation of glucose in an aqueous medium. Applied Nanoscience. 2021. https://doi.org/10.1007/s13204-021-01771-1
21. L.K. Patrylak, O.P. Pertko, A.V. Yakovenko, Yu.G. Voloshyna, V.A. Povazhnyi, M.M. Kurmach. Isomerization of linear hexane over acid-modified nanosized nickel-containing natural Ukrainian zeolites. Applied Nanoscience. 2021. https://doi.org/10.1007/s13204-021-01682-1.
22. Kalishyn Ye., Bychko I., Kameneva T., Skoblik O., Polunkin Ye., Strizhak P. Inhibition effect of the α-FeOOH nanoparticles in the benzyl alcohol oxidation.Journal of Cluster Science. 2021. DOI:10.1007/s10876-021-02056-x.
23. Shatursky O.Ya., Manoilov K.Yu., Gorbatiuk O.B., Usenko M.O., Zhukova D.A., Vovk A.I., Kobzar O.L., Trikash I.O., Borisova T.A., Kolibo D.V., Komisarenko S.V. The geometry of diphtheria toxoid CRM197 channel determined with thiazolium salts and nonelectrolytes. Biophys. J. 2021. V. 120, I. 12. P. 2577-2591.
24. Kobzar О. L., Shulha Y. V., Buldenko V. M., Mrug G. P., Kolotylo M. V., Stanko O. V., Onysko P.P., Vovk А. I. Alkyl and aryl α-ketophosphonate derivatives as photoactive compounds targeting glutathione-S-transferases. Phosphorus, Sulfur, and Silicon and the Related Elements. 2021. V. 196 (7). Р. 672-678.
25. Rogalsky S., Bardeau J.-Fr., Lyoshina L., Bulko O., Tarasyuk O., Dzhuzha O., Cherniavska T., Kremenitsky V., Kobrina L., Riabov S. New promising antimicrobial material based on thermoplastic polyurethane modified with polymeric biocide polyhexamethylene guanidine hydrochloride. Materials Chemistry and Physics. 2021. V.267. Р. 124682.
26. Orlovska I., Podolich O., Kukharenko O., Zaets I., Reva O., Khirunenko L., Zmejkoski D., Rogalsky S., Barh D., Tiwari S., Kumavath R., Góes-Neto A., Azevedo V., Brenig B., Ghosh P., de Vera J.-P., Kozyrovska N. Bacterial Cellulose Retains Robustness but Its Synthesis Declines After Exposure to a Mars-Like Environment Simulated Outside the International Space Station.Astrobiology. 2021. V. 21 (7). P. 706-717.
27. Rogalsky S., Bardeau J.-Fr., Makhno S., Tarasyuk O., Babkina N., Cherniavska T., Filonenko M., Fatyeyeva K. New polymer-electrolyte membrane for medium-temperature fuel cell applications based on cross-linked polyimide Matrimid and hydrophobic protic ionic liquid.Materials Today Chemistry. 2021. V. 20. P. 100453.
28. L. Muzychka, A. Voronkina, V. Kovalchuk, O. Smolii, M. Wysokowski, I. Petrenko, D. Youssef, I. Ehrlich, H. Ehrlich. Marine biomimetics: bromotyrosines loaded chitinous skeleton as source of antibacterial agents. Appl. Phys. A Mater. Sci Process. 2021. V. 127, № 1. P. 15.
29. L.V. Muzychka, E.V. Verves, I.O. Yaremchuk, A.M. Zinchenko, S.V. Shishkina, I.V. Semenyuta, D.M. Hodyna, L.O. Metelytsia, V.Kovalishyn, O.B. Smoliі.Synthesis, QSAR modeling, and molecular docking of novel fused 7-deazaxanthine derivatives as adenosine A2A receptor antagonists. Chem. Biol. Drug Des. 2021. V. 98. P. 1-8
30. Ключко С.В., Чумаченко С.А., Шаблыкин О.В., Броварец В.С. Синтез новых 1Н-пирроло-[3,4-c]¬пиридин-1,3(2Н)-дионов.ЖОХ. 2021. Т. 91, №3. С. 376-385.
31. Vydzhak R.N., Panchishin S.Ya., Kachaeva M.V., Pilyo S.G., Moskvina V.S., Shablykina O.V., Kozytskiy A.V., Brovarets V.S. A rapid synthetic approaches to the libraries of diversified 1,2-dihydrochromeno[2,3-c]pyrrole-3,9-diones and 3-(2-hydroxyphenyl)-4,5-dihydropyrrolo[3,4-c]pyrazole-6(1H)-ones.Molecular Diversity. 2021. 10.1007/s11030-021-10234-2.
32. Shcherbakova V., Dibchak D., Snisarenko M., Skalenko Ye., Denisenko A.V., Kuznetsova A.S., Mykhailiuk P.K. Bicyclic piperidines via [2+2] photocycloaddition. J. Org. Chem. 2021. V.86, №3. P. 2200-2209 doi/10.1021/acs.joc.0c02355.
33. Slyvchuk S., Pilyo S., Brovarets V., Kartsev V., Angeli A., Pinteala M., Petrou A., Geronikaki A., Supuran C. Chromene-containing aromatic sulfonamides with carbonic anhydrase inhibitory properties.Int. J. Mol. Sci. 2021. V.22, №10. P. 5082 https://doi.org/10.3390/ijms22105082.
34. Корний Ю.Е., Чумаченко С.А., Шаблыкин О.В., Русанов Э.Б., Броварец В.С. Новые гетероциклизации N’-замещенных N-(2,2-дихлор-1-цианоэтэнил)мочевин с алифатическими аминами.ЖОХ. 2021. –Т. 91, № 6. С. 841-846. doi/10.31857/s0044460х21060020.
35. Zhirnov V.V., Velihina Ye.S., Mitiukhin O.P., Brovarets V.S. Intrinsic drug potential of oxazolo[5,4-d]pyrimidines and oxazolo[4,5-d]pyrimidines.Chem. Biol. Drug Des. 2021. V.98, № 4. P. 561-581. doi:10.1111/cbdd.13911.
36. Merzhyievskyi D.O., Shablykin O.V., Shablykin O.V, Kozytskiy A.V., Rusanov E.B., Moskvina V.S., Brovarets V.S. Functionalized 5-amino-4-cyanooxazoles, their hetero and macrocyclic derivatives: preparation and synthetic applications.Eur. J. Org. Chem. 2021. doi.org/10.1002/ejoc.202100412
37. Angeli A., Kartsev V., Petrou A., Pinteala M., Vydzhak R., Panchishin S., Brovarets V., de Luca V., Capasso C., Geronikaki A., Supuran C. New sulfanilamide derivatives in corporating heterocyclic carboxamide moieties as carbonic anhydrase inhibitors. Pharmaceuticals. 2021. V. 14, № 8. P. 828 https://doi.org/10.3390/ph14080828
38. Kovalishyn V., Zyabrev V., Kachaeva M., Ziabrev K., Keith K., Harden E., Hartline C., James S., Brovarets V. Design of new imidazole derivatives with anti-HCMV activity: QSAR modeling, synthesis and biological testing.J. Comp.-Aided Mol. Des. 2021. V.35. P.1177-1187. doi.org/10.1007/s10822-021-00428-z.
39. Шаблыкин О.В., Чумаченко С.А., Броварец В.С. Взаимодействие новых N-(2,2-дихлор-1-цианоэтенил)амидов с алифатическими аминами.ЖОХ. 2021. Т.91, №9. С. 1315-1320.
40. Velihina E.S., Obernikhina N.V., Pilyo S.G., Kachkovsky O.D., Brovarets V.S. Synhesis, electronic structure and anti-cancer activity of the phenyl substituted pyrazolo[1,5-a][1,3,5]triazines.Current Org. Chem. 2021. V.25, №12. P. 1441-1454.
41. Maiko K., Merzhyievskyi D., Piryatinski Yu., Obernikhina N., Prostota Ya., Dmitruk I., Kachkovsky O., Brovarets V. Study of excited state relaxation by time-resolved spectroscopy in conjuigated substituted polyene bis-oxazoles.Structural Chem. 2021. V.32, №3. P. 977-987.
42. Angeli A., Kartsev V., Petrov A., Pinteala M., Brovarets V., Panchishin S., Vydzhak R., Geronikaki A., Supuran C.T. Carbonic anhydrase inhibition with sulfonamides incorporatiny pyrazole- and pyridazinecarboxamide moieties provides examples of isoform-selective inhibitors.Molecules. 2021. V. 26, № 22. P. 7023-7043. https://doi.org/10.3390/molecules26227023.
43. Ostapiuk Yu.V., Shehedyn M., Barabash O.V., Demydchuk B.A., Batsyts S., Herzberer C., Schmidt A. Bromoarylation of methyl 2-chloroacrylate under Meerwein conditions for the synthesis of substituted 3-hydroxyhiophenes.Synthesis. 2021. Doi: 10.1055/s-0040-1719849.
44. Shablykina O.V., Shylin S.V., Moskvina V.S., Ischenko V.V., Khilya V.P. Progress in the chemistry of aminoacid derivatives of isocoumarines and 3,4-dihydroisocoumarines.Chem. Nat. Compd. 2021. V. 57, № 2. P. 209-229. Doi:10.1007/s10600-021-03323-z.
45. Biletska I.M., Mrug G.P., Bondarenko S.P., Kondratyuk K.M., Prostota Y.O., Sviripa V.M., Frasinyuk M.S. Chemoselective synthesis of 3-trifluoromethylpyrazole-deoxybenzoin hybrids.J. Fluorine Chem. 2021. V.242. P. 109698.
46. Bondarenko S.P., Mrug G.P., Vinogradova V.I., Frasinyuk M.S. Synthesis of new conjugates of coumarins with anabasine and cytisine.Chem. Nat. Compd. 2021. V. 57, № 1. P. 9-13.
47. Shokol T.V., Moskvina V.S., Hlibov Y. K., Frasinyuk M.S., Khilya V.P. Synthesis of furoneoflavones modified by coumarin and (het)aroyl substituents.Chem. Nat. Compd. 2021. V. 57, № 1. P. 33-37.
48. Piryatinski Yu.P., Verbitsky A.B., Dmytruk A., Malynovskyi M.B., Lutsyk P.M., Rozhin A.G., Kachkovsky O.D., Prostota Ya.O., Kurdyukov V.V. Excited state relaxation in cationic pentamethine cyanines studied by time-resolved spectroscopy.Dyes Pigm. 2021. V. 193. P. 109539. https://doi.org/10.1016/j.dyepig.2021.109539.
49. Navozenko O., Yashchuk V., Kachkovsky O., Gudeika D., Butkute R., Slominskii Yu., Azovskyi V. Aggregate formation of boron-containing molecules in thermal vacuum deposited films. Materials. 2021. V. 14, №19. P. 5615. https://doi.org/10.3390/ma14195615.
50. Bashmakova N.V., Shaydyuk Ye.O., Dmytruk A.M., Swiergosz T., Kachkovsky O.D., Belfield K.D., Bondar M.V., Kasprzyk W. Nature of linear spectral properties and fast electronic relaxations in green fluorescent pyrrolo[3,4-c]pyridine derivative.Int. J. Mol. Sci. 2021. Vol. 22, №11. P. 5592. https://doi.org/10.3390/ijms22115592.
51. Shaydyuk Ye.O., Bashmakova N.V., Dmytruk A.M., Kachkovsky O.D., Koniev S., Strizhak A.V., Komarov I.V., Belfield K.D., Bondar M.V., Babii O. Nature of fast relaxation processes and spectroscopy of a membrane-active peptide modified with fluorescent amino acid exhibiting excited state intramolecular proton transfer and efficient stimulated emission.ACS Omega. 2021. V. 6, № 15. P. 10119-10128. https://doi.org/10.1021/acsomega.1c00193.
52. A.O. Adejuwon, O.D. Odeleye, O.A. Odewale, V.A. Tsygankova, M.V. Donova. A Medicinal Plant’s Extract Effective on Osteoarthritis.Biomedicine and Nursing. 2021. V.7 (1). P. 26-28. doi:10.7537/marsbnj070121.04.
53. A. Adejuwon, V. Tsygankova, M. Donova, O. Odeleye. A Medicinal Plant’s Extract Effective on Tuberculosis in Cases of Osteotic Transformation in Tropical Nigeria. Cancer Biology. 2021. V. 11 (2). P. 106-108. doi:10.7537/marscbj110221.03.
54. Vasylyuk S.V., Suprun A.D., Shmeleva L.V., Kachkovsky O.D. Configuration of charge waves in polymethine linear dye systems. Springer proceedings in physics. 2021. V. 246. P. 189-201.
55. M.D. Aksylenko, V.A. Yevdokymenko, T.V. Tkachenko, D.S. Kamenskyh, V.I. Kashkovsky.Effective organo-mineral fertilizers of prolonged action from the processed organo-containing wastes of various origin. Proceeding Book of III Balkan agricultural congress. August 30-September 1, 2021. Edirne, Turkey. P. 554-564.
56. V. Bratishko, T. Tkachenko, S. Shulha, O. Tigunova. Results of composition analysis of non-grain part of major field crops in Ukraine. Proceeding Book of 20th International Scientific Conference Еngineering for rural development. V. 20. May 26-28, 2021. Jelgava, Latvia. Р. 584-588. https://doi.org/10.22616/ERDev.2021.20.TF125.
57. Starodubtseva A., Kalachova T., Iakovenko O., Stoudková V., Zhabinskii V., Khripach V., Ruelland E., Martinec J., Burketová L., Kravets V. BODIPY Conjugate of Epibrassinolide as a Novel Biologically Active Probe for іn vivo Imaging. International Journal of Molecular Sciences. 2021. V. 22 (3599). Р. 1-12.
58. Pokotylo I., Hodges M., Kravets V., Ruelland E. A ménage à trois: Salicylic acid, growth inhibition and immunity. Trends in plant Sciences. 2021. TRPLSC2223 https://doi.org/10.1016/j.tplants.2021.11.008.
59. O.O. Grygorenko, V.S. Moskvina, I. Kleban, O.V. Hryshchyk. Synthesis of saturated and partially saturated heterocyclic boronic derivatives. Tetrahedron. 2021. https://doi.org/10.1016/j.tet.2021.132605.

2020 р.

Розділи в зарубіжних монографіях

1. Romanenko V.D. Rings containing group 15 elements.Ref. Mod. Chem. Molecular Sciences. Elsevier. 2020. Р.1-36.
2. Parkhomenko Y., Vovk A., Protasova Z. Vitamin B1 and the pyruvate dehydrogenase complex.In Molecular Nutrition. Vitamins. Academic Press. 2020. P. 185-206.
3. Poda G., Tanchuk V. Computational Methods for the Discovery of Chemical Probes.The Discovery and Utility of Chemical Probes in Target Discovery. RSC Publishing. 2020. P. 39-68.
4. V.A. Tsygankova, K.B. Blyuss, E.N. Shysha, L.A. Biliavska, G.A. Iutynska, Y.V. Andrusevich, S.P. Ponomarenko, A.I. Yemets, Y.B. Blume. Using Microbial Biostimulants to Deliver RNA Interference in Plants as an Effective Tool for Biocontrol of Pathogenic Fungi, Parasitic Nematodes and Insects.In Monograph «Research Advances in Plant Biotechnology». Series: Plant Science Research and Practices. Chapter 6. Nova Science Publishers, Inc. USA. 2020. 375 p. P. 205-319.
5. A.O. Adejuwon, V.A. Tsygankova. α-Amylase Production by Toxigenic Strains of Aspergillus and Penicillium.In Monograph “Aflatoxin B1 Occurrence, Detection and Toxicological Effects” Ed. by Xi-Dai Long. IntechOpen, 2020. P. 1-22.

Публікації в зарубіжних виданнях

1. A.О. Kolodiazhna, O.I. Kolodiazhnyi. Asymmetric Electrophilic Reactions in Phosphorus Chemistry. Symmetry. 2020. V.12, № 1. Р. 108-159.
2. A.О. Kolodiazhna, А.I Skliarov, A.A. Slastennikova, O.I Kolodiazhnyi. Asymmetric Synthesis of (S,R)- and (R,R)-Methiin Stereoisomers. Phosph., Sulf., Silicon and Relat. Elem. 2020. V.195. P. 713-717.
3. T. Tkachenko, V. Yevdokymenko, D. Kamenskyh, Y. Sheludko, V. Povazhny, V. Kashkovsky. Physico-chemical properties of biogenic SiO₂ nanoparticles obtained from agriculture residue. Applied Nanoscience. 2020. V. 10, № 12. P. 4617 – 4623.
4. Tigunova O.O., Kamenskyh D.S., Tkachenko T.V., Yevdokymenko V.A., Kashkovskiy V.I., Rakhmetov D.B., Blume Ya.B., Shulga S.M.. Biobutanol Production from Plant Biomass. The Open Agriculture Journal. 2020. V. 14. P. 187-197.
5. V. Kovalishyn, D. Hodyna, V.O. Sinenko, V. Blagodatny, I. Semenyuta, S. R. Slivchuk, V. Brovarets, G. Poda, L. Metelytsia. Hybrid Design of Isonicotinic Acid Hydrazide Derivatives: Machine Learning Studies, Synthesis and Biological Evaluation of their Antituberculosis Activity. Current Drug Discovery Technologies. 2020. V. 17. Р. 365-375.
6. M. Trush, V. Kovalishyn, D. Hodyna O. Golovchenko S. Chumachenko I. Tetko V. Brovarets L. Metelytsia. In silico and in vitro studies of a number PILs as new antibacterials against MDR clinical isolate Acinetobacter baumannii. Chem Biol Drug Des. 2020. V. 95. Р. 624-630.
7. N. Abramenko, L. Kustova, L. Metelytsia, V. Kovalishyn, I. Tetko, W. Peijnenburg. A review of recent advances towards the development of QSAR models for toxicity assessment of ionic liquids. Journal of Hazardous Materials. 2020. V. 384. 121489. Р. 1-14.
8. M. M.Trush, I. Semenyuta, D. Hodyna, A. Ocheretniuk, S. Vdovenko, S. Rogalsky, L. Kalashnikova, V. Blagodatnyi, O. Kobzar, L. Metelytsia. Functionalized imidazolium-based ionic liquids: biological activity evaluation,toxicity screening, spectroscopic, and molecular docking studies. Medicinal Chemistry Research. 2020. V. 29. Р. 2181-2191.
9. L. Metelytsia, M. Trush, I. Semenyuta, S. Rogalsky, O. Kobzar, L. Kalashnikova, V. Blagodatny, D. Hodyna. Ionic Liquids with Anti-Candida and Anticancer Dual Activity as Potential N-Myristoyltransferase Inhibitors. Current Bioactive Compounds. 2020. V.16, №7. Р. 1036-1041.
10. Ghamrawi S., Bouchara J.-Ph., Corbin A., Rogalsky S., Tarasyuk O., Bardeau J.-Fr. Inhibition of fungal growth by silicones modified with cationic biocides. Materials Today Communications. 2020. V. 22. Р. 100716.
11. Fatyeyeva, K., Rogalsky, S., Makhno, S., Tarasyuk, O., Soto Puente, J.A. Marais, S. Polyimide/Ionic Liquid Composite Membranes for Middle and High Temperature Fuel Cell Application: Water Sorption Behavior and Proton Conductivity. Membranes.2020. V.10. Р.82.
12. Pokotylo I., Hellal D., Bouceba T., Hernandez-Martinez M., Kravets V., Leitao L., Espinasse C., Kleiner I., Ruelland E.. Deciphering the Binding of Salicylic Acid to Arabidopsis thaliana Chloroplastic GAPDH-A1. International Journal of Molecular Sciences. 2020. V. 21, №13. Р. 4678.
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14. Bugera M.Ya, Tarasenko K.V., Kondratov I.S., Gerus I. I, Vashchenko B.V., Ivasyshyn V.E. Grygorenko O.O.. (Het)aryl difluoromethyl-substituted β-alkoxyenones: synthesis and heterocyclizations. European Journal of Organic Chemistry. 2020. V. 9. Р. 1069-1077.
15. Malashchuk A., Chernykh, A.V., Hurmach V.V., Platonov M.O., Onopchenko O., Zozulya S., Daniliuc C.G., Dobrydnev A.V., Kondratov I.S., Moroz Yu.S. Grygorenko O.O. Synthesis, biological evaluation, and modeling studies of 1,3- disubstituted cyclobutane-containing analogs of combretastatin A4. Journal of Molecular Structure. 2020. V. 1210. Р. 128025-128033.
16. Stepaniuk O.O., Vashchenko B.V., Matvienko V.O., Kondratov I.S., Tolmachev A.A., Grygorenko O.O. Reactions of cyclic β-alkoxyvinyl α-keto esters with heteroaromatic NCC-binucleophiles. Chemistry of Heterocyclic Compounds. 2020. V. 56, № 3. Р. 377-385.
17. Stepaniuk O.O, Rudenko T.V., Vashchenko B.V., Matvienko V.O., Kondratov I.S., Tolmachev A.A., Grygorenko O.O. Synthesis of Fused Pyridine Carboxylates by Reaction of β-Alkoxyvinyl Glyoxylates with Amino Heterocycles. Synthesis. 2020. V. 52, № 13. Р. 1915-1926.
18. Feskov I.O., Golub B.O., Vashchenko B.V, Levterov V. V., Kondratov I.S., Grygorenko O.O., Haufe G.. GABA Analogues and Related Mono‐/Bifunctional Building Blocks Derived from the Fluorocyclobutane Scaffold. European Journal of Organic Chemistry. 2020. V. 30. Р. 4755-4767.
19. Klipkov A.A., Sorochinsky A.E., Tarasenko K.V., Rusanova J.A., Gerus I.I. Synthesis of trifluoromethyl and trifluoroacetyl substituted dihydropyrrolizines and tetrahydroindolizines. Tetrahedron Lett. 2020. V. 61. P. 151633.
20. Gerus I.I, Zhuk Y.I, Kacharova L.M, Röschenthaler G., Shaitanova E.N., Sorochinskii A.E., Vdovenko S. I., Wojcik Y.. Uncommon fluorination of enones with xenon difluoride. Journal of Fluorine Chemistry. 2020. V. 229. Р. 109413.
21. Trofymchuk S., Bugera M., Klipkov A., Razhyk B., Semenov S., Tarasenko K., Starova V., Zaporozhets O., Tananaiko O., Alekseenko A., Pustovit Y., Kiriakov O., Gerus I., Tolmachev A., Mykhailiuk P.. Deoxofluorination of (Hetero) aromatic Acids. The Journal of Organic Chemistry. 2020. V. 85, № 5. Р. 3110-3124.
22. Trofymchuk S.A, Kliukovskyi D.V., Semenov S.V., Khairulin A.R., Shevchenko V.O., Bugera M.Y., Tarasenko K.V., Volochnyuk D.M., Ryabukhin S.V. Semi-Industrial Fluorination of β-Keto Esters with SF4: Safety vs Efficacy. Synlett. 2020. V. 31, № 06. Р. 565-574.
23. Vretik L.O., Noskov Y.V., Ogurtsov N.A., Nikolaeva O.A., Shevchenko A.V., Marynin A.I., Kharchuk M.S., Chepurna O.M., Ohulchanskyy T.Y., Pud A.A. Thermosensitive ternary core–shell nanocomposites of polystyrene, poly(N-isopropylacrylamide) and polyaniline. Applied Nanoscience. 2020. V. 10, № 12. P. 4951-4964.
24. Rudenko R.M., Voitsihovska O.O., Poroshin V.M., Petrychuk M.V., Pavlyuk S.P., Nikolenko A.S., Ogurtsov N.A., Noskov Y., Sydorov D.O., Pud A.A.. Specific interactions and charge transport in ternary PVDF/polyaniline/MWCNT nanocomposite films(Article). Composites Science and Technology. 2020. V. 198. Р. 108284.
25. Kislyuk V., Kotrechko S., Trachevskij V., Melnyk A., Pud A., Ogurtsov N., Noskov Y., Osiponok M., Lytvyn P., Dzyazko Y., Akhmadaliev S., Kentsch U., Krause M., Facsko S. Impact of low energy ion beams on the properties of rr-P3HT films(Article). Applied Surface Science. 1 January 2021. V. 535. Р. 147619.
26. Hamouda Z., Wojkiewicz J.L., Pud A.A., Bergheul S., Lasri T.. Broadband dielectric characterization of flexible substrates using organic conductive polymer microstrip lines. Microwave and Optical Technology Letters. 2020. V. 62, № 2. P. 688-695.
27. Binnewerg B., Schubert M., Voronkina A., Muzychka L., Wysokowski M., Petrenko Ia., Djurović M., Kovalchuk V., Tsurkan M., Smolii O.B., Ehrlich H.. Marine biomaterials: Biomimetic and pharmacological potential of cultivated Aplysina aerophoba marine demosponge. Materials Science and Engineering C. 2020. V. 109. Р. 110566.
28. Mezhenska O., Rebriev A., Kobzar O., Zlatoust N., Vovk A., Parkhomenko Yu. Non-coenzyme properties of thiamine: evaluation of binding affinity to malate dehydrogenase isoforms. Biotechnologia Acta. 2020. V. 13, № 4. P. 26-38.
29. Shokol T.V., Gorbulenko N.V., Frasinyuk M.S., Khilya V.P.. Synthesis of 7-Hydroxy-8-Methyl-4′-Methoxy-6-Formylisoflavone and Linear Hetarenochromones Based on It. Chem. Nat. Compd. 2020. V.56, № 3. P. 420-422.
30. Tang B., Frasinyuk M.S., Chikwana V.M., Mahalingan K.K., Morgan C.A., Segvich D.M., Bondarenko S.P., Mrug G.P., Wyrebek P., Watt D.S., DePaoli-Roach A.A., Roach P.J., Hurley T.D. Discovery and Development of Small-Molecule Inhibitors of Glycogen Synthase. J. Med. Chem. 2020. V.63, № 7. P. 3538-3551.
31. Shokol T.V., Gorbulenko N.V., Frasinyuk M.S., Khilya V.P. Synthesis of Benzofurans Modified by Coumarin and Pyrazole Heterocycles. Chem. Nat. Compd., 2020. V.56. P. 1060-1063.
32. Bondarenko S.P., Makarenko O.G., Vinogradova V.I., Frasinyuk M.S. Synthesis of 7-(N-12-Cytisinylpropoxy)Isoflavones. Chem. Nat. Compd. 2020. V.56 P. 1040-1043.
33. Golovchenko O.V., Abdurakhmanova E.R., Vladimirov S.O., Brusnakov M.Y., Krupoder T.O., Sukhoveev V.V., Rusanov E.B., Vydzhak R.N., Brovarets V.S. Interaction of 1-acylamino-2,2-dichloroethenyl(triphenyl)phosphonium chlorides with alkanolamines. Phosph. Sulph. Silicon and Relat. Elem. 2020. V.195, №10. P. 848-857.
34. Konovalenko A.S., Shablykin O.V., Brovarets V.S., Shablykina O.V., Moskvina V.S., Kozytskiy A.V.. 3-Hetarylisocoumarins in the synthesis of 1‑functionalized 3-hetarylisoquinolines. Chem. Het. Compd. 2020. V.56, № 8. P. 1021-1029.
35. Omelian T.V., Ostapchuk E.N., Dobrydnev A.V., Malets Y.S., Brovarets V.S., Grygorenko O.O. Strategy for the synthesis of 2,2-disubstituted 8‑azachromanones via Horner-Wadsworth_Emmons. Chem. Het. Compd. 2020. V.56, № 2. P. 213-218.
36. Abdurakhmanova E.R., Brusnakov M.Y., Golovchenko O.V., Pilyo S.G., Velychko N.V., Hariden E.A., Prichard M.N., James S.H., Zhirnov V.V., Brovarets V.S. Synthesis and in vitro anticitomegalovirus activity of 5-hydroxyalkylamino-1,3-oxazoles derivatives. Med. Chem. Res., 2020. V.29, № 9. P. 1669-1675.
37. Выджак Р.Н., Панчишин С.Я., Броварец В.С.. Применение никелевых комплексов 1,3‑дикарбонильных соединений для синтеза конденсированых систем с ядром 4‑аминопиразола. ЖОХ. 2020. T. 90, №8. С. 1231-1239.
38. L.M. Potikha, V.S. Brovarets. Synthesis of new antineoplastic agents based on imadazo[2,1-a]pyridine. Chem. Heterocycl. Compd. 2020. V.56, № 11. P. 1460-1464.
39. Potikha L.M., Brovarets V.S.. Synthethis of imidazole[2,1-b][1,3]thiazoles – potential anticancer agents derived from p-bromodipnones. Chem. Heterocycl. Compd. 2020. V.56, № 8. P. 1073-1077.
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41. Grygorenko O.O., Hutskalova V., Moskvina V.S. Bicyclic 6-6 systems with one bridgehead (ring junction) nitrogen atom: three extra heteroatoms (2:1). Chapter in collection: “Reference module in chemistry, molecular sciences and chemical engineering”. 2020.
42. Tsygankova V.A., Andrusevich Ya.V., Shtompel O.I., Pilyo S.G., Kornienko A.M., Brovarets V.S. The new plant growth regulators based on derivatives of oxazole and oxazolopyrimidine. World J. Pharm. Toxicol. 2020. V.3, № 2. P. 1-5.
43. Nizhenkovska I.V., Matskevych K.V., Golovchenko O.V., Golovchenko O.I.. Synthesis and pharmacological trials of new phosphorylated oxazole derivatives antihypertensive properties. Maced. Pharm. Bull. 2020. V.66, № 1. P. 51-52.
44. Velihina Ye., Scattolin T., Bondar D., Pil’o S.,Obernikhina N.,Kachkovskyi O.,Semenyuta I., Caligiuri I., Rizzolio F., Brovarets V.,Karpichev Ye.,
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46. Obernikhina N., Pavlenko O., Kachkovsky A., Brovarets V.. Quantum-chemical and experimental estimation of non-bonding level (Fermi level) and π‑electron afinity of conjugated systems. Polycycl. Arom. Comp. 2020. P. 1-10.
47. Blyuss K.B., Al Basir F., Tsygankova V.A. Control of mosaic disease using microbial biostimulants: insights from mathematical modelling. Ricerche Mat. 2020. V.69. P. 437-455.
48. Adejuwon A.O., Tsygankova V.A., Obayemi O.S., Ogundare H.O. The Anti-microbial Efficacy and Phytochemical Analysis of the Root Bark of Uvaria chamea. Nature and Science. 2020. V.18, № 5. P. 73-80.
49. Adejuwon A.O., Obayemi O.S., Odeleye O.D., Tsygankova V.A. COVID-19 in Nigeria, West Africa: An Update. Advances in Bioscience and Bioengineering. 2020. V.8, № 2. P. 1-12.
50. Davydenko I.G., Slominskiy Yu.L., Obernikhina N.V., Kachkovsky A.D., Tolmachev A.. Infrared Polyene Radical-Cation Derived from 7,8-Dihydrobenzo[c,d]Furo[2,3-f]Indole: Synthesis, Spectra and Nature of Electron Transitions. Chemistry Select. 2020. V.5. P. 674-681.
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52. Tsygankova V., Voloshchuk I., Andrusevich Y., Shtompel O., Kopich V., Klyuchko S., Brovarets V. The influence of the derivative of pyrimidine – Methyur on the yield of the maize, beet and oats plants. Збірник статей «Topical issues of the development of modern science» за матеріалами 8-ї Міжнародної наукової та практичної конференції. Видавництво “ACCENT”, Софія, Болгарія. 2020. P. 514-523.
53. Adejuwon A.O., Obayemi O.S., Odeleye O.D., Tsygankova V.A., Thonda O.. Inhibitory Actions of a Medicinal Plants’ Extract on SARS-CoV-2 and COVID-19. Cancer Biology. 2020. V.10, № 3. P. 1-3.
54. Adejuwon A.O., Donova M.V., Obayemi O.S. Tsygankova V.A. SARS-CoV-2 and COVID-19 phyto-activity in individuals with hematopoietic stem cell transplants. Stem Cell. 2020. V.11, № 3. P. 39-41.
55. Adejuwon A.O., Odeleye O.D., Odewale O.A., Obayemi O.S., Tsygankova V.A., Thonda O.,Donova M.V.. Effective medicinal plants’ extract on ability to properly empty bladder in patients with benign prostatic hyperplasia and Escherichia coli infection. Stem Cell. 2020. V.11, № 3. P. 42-44.

2019 р.

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3. Kachaeva M.V., Hodyna D.M., Obernikhina N.V., Pilyo S.G., Kovalenko Y.S., Prokopenko V.M., Kachkovsky O.D., Brovarets V.S. Dependence of the anticancer activity of 1,3-oxazole derivatives on the donor/acceptor nature of his substitues. Journal of Heterocyclic Chemistry. 2019. Vol. 56 (11). P. 3122-3134. DOI: 10.1002/jhet.3711.
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4. Shaydyuk Y.O., Boyko O.P., Kachkovsky O.D., Slominsky Y.L., Bricks J.L., Belfield K.D., Bondar M.V. Electronic nature of new styryl dye bases: Linear photophysical, photochemical, and transient absorption spectroscopy studies. Dyes and Pigments. 2019. Vol. 170. DOI: 10.1016/j.dyepig.2019.107582.
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6. Mrug G.P., Biletska I.M., Bondarenko S.P. Sviripa V.M., Frasinyuk M.S. Trifluoroacetylation of 2-Methyl- and 2-Ethylchromones: A Convenient Access to 2-Trifluoroacetonyl Chromones. ChemistrySelect. 2019. Vol. 4 (39). P. 11506-11510. DOI: 10.1002/slct.201903629.
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    Lutynska G.O., Biliavska L.O., Babych O.A., Tsygankova V.A., Babych A.G. The Monograph “Plant protection and bioregulation in modern agriculture” / Ed. “Diamond trading tour” Warszawa. Poland, 2019.- 100 p. ISBN: 978-83-66030-73-2.
    
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10. Kovalishyn V., Grouleff J., Semenyuta I., Sinenko V.O., Slivchuk S.R., Hodyna D., Brovarets V., Blagodatny V., Poda G., Tetko I.V., Metelytsia L.. Rational design of isonicotinic acid hydrazide derivatives with anti-tubercular activity: Machine learning, molecular docking, synthesis and biological testing.. Chem. Biol. & Drug Des.- 2018.- V.92 (№1).- P. 1272-1278.
11. Kachaeva M.V., Hodyna D.M., Semenyuta I.V., Pilyo S.G., Prokopenko V.M., KovalishynV.V., Metelytsia L.O., Brovarets V.S.. Design, synthesis and evaluation of novel sulfonamides as potential anticancer agents.. Comput. Biol. Chem.- 2018.- V.10 (№74).- P. 294-303.
12. L.K. Patrylak, M.M. Krylova, O.P. Pertko, Yu.G. Voloshyna . Linear Hexane Isomerization over Ni-Containing Pentasils . J. Porous Mater.- 2018 https://doi.org/10.1007/s10934-018-0685-1.
13. Iu. Little, E. Alorkpa, V. Khan, V. Povazhnyi, A.Vasiliev. Efficient porous adsorbent for removal of cesium from contaminated water. J. Porous Mater.- 2018.- Vol. 244.- Р. 55-63.
14. P.Le. Maout, J.-L. Wojkiewicz, N. Redon, C. Lahuec, F. Seguin, L. Dupont, S. Mikhaylov, Yu. Noskov, N. Ogurtsov, A. Pud. Polyaniline nanocomposites based sensor array for breath ammonia analysis. Portable e-nose approach to non-invasive diagnosis of chronic kidney disease. Sensors and Actuators B.- 2018.- Vol. 274.- Р. 616-626.
15. Z. Hamouda, J.L. Wojkiewicz, A.A. Pud, L. Kone, S. Bergheul, T. Lasri. Magnetodielectric Nanocomposite Polymer-Based Dual-Band Flexible Antenna for Wearable Applications. IEEE Transactions on Antennas and Propagation.- 2018.- Vol. 66(7).- Р. 3271-3277.
16. Ogurtsov N.A., Bliznyuk V.N., Mamykin A.V., Kukla O.L., Piryatinski Yu.P., Pud A.A.. Improved Structural and Electronic Properties of Poly(3-Methylthiophene) in Nanocomposites with Poly(Vinylidene Fluoride). Effect of an Electroactive Template”. Physical Chemistry Chemical Physics.- 2018.- Vol. 20.- Р. 6450-6461.
17. Trepyadko D., Korzh R, Kremenetskii V, Nasieka Iu., Naseka V., Stanovyi O., Bortyshevskii V.. Graphitic carbon sub-nitride: synthesis, structure, electron and proton transport, phо-toluminescence and thermoelectric proper-ties. Materials Chemistry and Physics. – 2018. – Vol. 209. – P. 95-106.
18. I.O. Yaremchuk, L.V. Muzychka, O.B. Smolii, O.V. Kucher, S.V. Shishkina. Synthesis of novel 1,2-dihydro-pyrrolo[1,2-a]pyrazin-1(2H)-one derivatives. Tetrahedron Lett.- 2018.- Vol. 59, №5.- P.442-444 19. A.M. Zinchenko, L.V. Muzychka, O.V. Kucher, I.V. Sadkova, P.K. Mykhailiuk, O.B. Smolii. One-Pot Synthesis of 6-Aminopyrido[2,3-d]pyrimidin-7-ones. Eur. J. Org. Chem.- 2018.- № 47 DOI: 10.1002/ejoc.201801204.
20. Tarasenko K.V., Romanenko V.D., Sorochinsky A.E.. Condensation of diethyl fluoromethylphosphonate with esters: An alternative synthetic route to diethyl ?-fluoro-?-ketophosphonates. J. Fluorine Chem.- 2018.- Vol. 211.- Р. 124-128.
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22. Khlebnicova T.S., Piven Yu.A., Isakova V.G., Baranovsky A.V., Lakhvich F.A., Sorochinsky A.E., Gerus I.I. Regioselective Synthesis of Polyfluoroalkyl Substituted 6,7-Dihydrobenzisoxasolones. Journal of Heterocyclic Chemistry.- 2018.- Vol. 55.- Р. 1791-1797 doi.org/10.1002/jhet.3218.
23. Romanenko V.D., Kukhar V.P.. Phosphonate analogues of nucleoside polyphosphates. Arkivoc.- 2018.- part i.- Р.1-49 https://doi.org/10.24820/ark.5550190.p010.183.
24. Kondratov I.S., Bugera M.Ya., Tolmachova N.A., Daniliuc C.G., Haufe G.. Straightforward synthesis of fluorinated amino acids by Michael addition of ethyl bromodifluoroacetate to ?, ?-unsaturated ?-amino acid derivatives. Journal of Fluorine Chemistry.- 2018.- Vol. 211.- Р. 100-108.
25. Borysko P., Moroz Y.S., Vasylchenko O.V., Hurmach V.V., Starodubtseva A., Stefanishena, N. Nesteruk K., Zozulya S., Kondratov I.S., Grygorenko O.O.. Straightforward hit identification approach in fragment-based discovery of bromodomain-containing protein 4 (BRD4) inhibitors. Bioorganic & medicinal chemistry.- 2018.- Vol. 26, № 12.- Р. 3399-3405.
26. Kondratov I.S., Tolmachova N.A, Haufe G.. Diels–Alder Reaction in the Synthesis of Fluorinated (Hetero) Aromatic Compounds. European Journal of Organic Chemistry.- 2018.- (27-28).- Р. 3618-3647
27. Gerus I.I., Balabon O.A., Pazenok S.V., Lui N., Kondratov I.S., Tarasenko K.V., Shaitanova E.N., Ivasyshyn, V.E. Kukhar V.P. Synthesis and Properties of Polyfunctional Cyclic ?-Alkoxy-Unsaturated Ketones Based on 4-Methylene-1,3-dioxolanes. European Journal of Organic Chemistry.- 2018.- (27-28).- Р. 3853-3861.
28. Tolmachova N.A., Kondratov I.S., Dolovanyuk V.G., Pridma S.O., Chernykh A.V., Daniliuc C.G., Haufe G.. Synthesis of new fluorinated proline analogues from polyfluoroalkyl ?-ketoacetals and ethyl isocyanoacetate. Chemical Communications.- 2018.- Vol. 54 (69).- Р. 9683-9686.
29. Zyabrev V.S., Babii S.B.. Reactions of 5-mesyl-2-phenyl-4-tosyloxazole with N-, C-, and S-nucleophiles. Chem. Heter. Comp.- 2018. – Vol. 54, № 1. – Р. 93-95.
30. Frasinyuk M.S., Zhang W., Wyrebek P., Yu T., Xu X., Sviripa V.M., Bondarenko S.P., Xie Y., Ngo H.X., Morris A.J., Mohler J.L., Fiandalo M.V., Watt D.S., Liu C.. Developing antineoplastic agents that target peroxisomal enzymes: cytisine-linked isoflavonoids as inhibitors of hydroxysteroid 17-beta-dehydrogenase-4(HSD17B4). Organic, Biomolecular Chemistry.- 2017. – Vol. 15.- P.7623-7629.
31. Iakovyshen R.S., Kurdyukov V.V., Brusentsov V.A., Pavlenko E.L., Dmytrenko O.P., Kulish M.P., Tolmachev O.I., Kachkovsky O.D.. Spectral and quantum-chemical study of absorption of merocyanines derivatives of cyclohexadienon. J.Advanc.Phys., 2017. – Vol.6. – P. 514-523.
32. Выджак Р.Н., Панчишин С.Я., Броварец В.С.. Алкилирование 1-алкил-3-метил-1,4-дигидропиразоло[3,4-c]-пиразолов эфирами галогенкарбоновых кислот. ЖОХ.- 2018. – Т.88, № 2.- С.242-254.
33. Solomyannyi R., Slivchuk S., Smee D., Choi J., Rusanov E., Zhirnov V., Brovarets V.. In vitro activity of the novel pyrimidines and their condensed derivatives against poliovirus. Current Bioactive Comp. 2018. – Vol.14, № 14. – P. 1-9.
34. Kachkovsky A., Obernikhina N., Prostota Y., Naumenko A., Melnyk D., Yashchuk V.. Estimation of the basicity of the donor strength of terminal groups in cationic polymethine dyes. J. Molec. Structure.- 2018. – Vol.1154. – P. 606-618.
35. Sinenko V.O., Slivchuk S.R., Brovarets V.S.. Lithiation of 2-Bromo-4-(1,3-dioxolan-2- yl)-13-thiazole. Current Chem. Letters.- 2018. – Vol. 8. – P.1-8.
36. Kachaeva M.V., Pilyo S.G., Demydchuk B.A., Prokopenko V.M., Zhirnov V.V., Brovarets V.S.. 4-Cyano-1,3-oxazole-5-sulfonamides as Novel Promising Anticancer Lead Compounds. Intern. J. Curr. Res.- 2018. – Vol. 10, № 5. – P. 69410-69425.
37. Tsygankova V., Andrusevich Y., Shompel O., Kopich V., Solomyanny R., Bondarenko O., Brovarets V.. Phytohormone-like effect of pyrimidine derivatives on regulation of vegetative growth of tomato. International J. of Botany Studies.- 2018. – Vol. 3, № 2. – P. 91-102.
38. Tsygankova V., Andrusevich Y., Kopich V., Shtompel O., Veligina Ye., Pilyo S., Kachaeva M., Kornienko A., Brovarets V.. Application of Oxazole and Oxazolopyrimidine as New Effective Regulatores of Oilseed Rape Growth. Sch. Bull.- 2018. – Vol. 4, № 3. – P. 301-312.
39. Шаблыкин О.В., Волощенюк М.А., Броварец В.С.. Синтез новых 2-(оксиран-2-ил)-1,3-оксазолов. ЖОХ.- 2018. – Т. 88, № 7. – С. 1207-1210.
40. Chalyk B.A., Hrebeniuk K.V., Gavrilenko K.S., Shablykin O.V., Yanshyna O.O., Bash D., Mykhailik P.K., Liashuk O.S., Grygorenko O.O.. Synthesis of Bi- and Polyfunctional Isoxazoles from Amino Acid-Derived Halogenoximes and Active Methylene Nitriles. Eur. J. Org. Chem.- 2018. -Vol. 22. – P. 2753-2761.
41. Popova A.V., Bondarenko C.P., Frasinyuk M.S., Wen Zhang, Xie Yanji, Martin Zachary M., Cai Xianfeng, Fiandalo Michael V., Mohler James L., Liu Chunming, Watt David S., Sviripa V.M.. Efficient synthesis of aurone Mannich bases and evaluation of their antineoplastic activity in PC-3 prostate cancer cells. Chemical Papers, 2018. – Vol. 72, № 10. – P. 2443-2456.
42. Kachaeva M., Pilyo S., Popilnichenko S., Kornienko A., Rusanov E., Prokopenko V., Zyabrev V., Brovarets V.. Synthesis of fused heterocycles from 2-aryl-5-(chlorosulfonyl)oxazole-4-carboxylates and ?-aminoakoles involving the Smiles rearrangement. Current Chem. Letters.- 2018. – Vol. 7, № 4. – P. 101-110.
43. Brovarets V.S., Golovchenko O.V., Rusanov E.B., Rusanova J.A.. Crystal structure of diethyl {2,2,2-tri¬chloro-1-[2-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)-4-methyl¬pentanamido]¬eth-yl}phospho¬nate. Acta Cryst.- 2018. – Vol. E74. – P. 915-917 https://doi.org/10.1107/S2056989018008277.
44. Tsygankova V.A., Andrusevich Ya.V., Shtompel O.I., Pilyo S.G., Kornienko A.M., Brovarets V.S.. Using of [1,3]oxazolo[5,4-d]pyrimidine and N-sulfonyl substituted of 1,3-oxazole to improve the growth of soybean seedlings. Chem. Res. J.- 2018. – Vol. 3 (2).- P. 165-173.
45. Velihina Ye., Kachaeva M.V., Pilyo S.G., Zhirnov V.V., Brovarets V.S.. Synthesis, Characterization, and Vitro Anticancer Evaluation of 7-Piperazin-substituted [1,3]oxazolo[4,5-d]pyrimidines. Der Pharma Chemica.- 2018. – Vol. 10, № 9. – Р. 1-10.
46. Мруг Г.П., Бондаренко Н.В., Бондаренко С.П., Фрасинюк М.С.. Реакционная способность конденсированных производных изофлавонов по отношению к гидразину. Химия природных соединений.- 2018. – Т.54, №4.- С. 654-659.
47. Бондаренко С.П., Мруг Г.П., Кондратюк К.М., Фрасинюк М.С.. Аминометилирование афроморсина, кладрастина и их 2-метилпроизводных. Химия природных соединений.- 2018. – Т.54, № 4. – С. 660-664.
48. Tsygankova V.A., Andrusevich Ya.V., Shtompel O.I., Pilyo S.G., Kornienko A.M., Brovarets V.S.. Acceleration on vegetative growth of wheat (Triticum aestivum L.) using [1,3] oxazolo[5,4-d]pyrimidine and N-sulfonyl substituted 1,3-oxazole. Pharm. Chem. J., 2018. – Vol.5, № 2. – P. 167-175.
49. Bogolyubsky A., Savych O., Zhemera A., Khomenko D., Brovarets V., Moroz Yu., Vybornyi M.. A facile one-pot parallel synthesis of 3-amino-1,2,4-triazoles. ACS Combinatorial Science, 2018. – Vol. 20, № 7.– P. 461-466.
50. Kachaeva M.V., Pilyo S.G., Zhirnov V.V., Brovarets V.S. Synthesis, characterization, and in vitro anticancer evaluation of 2- substituted 5-arylsulfonyl-1,3-oxazole-4-carbonitriles. Med. Chem. Res.- 2018. – Vol. 22, № 12 https://doi.org/10.1007/s00044-018-2265-y.
51. Mrug G.P., Demydchuk B.A., Bondarenko S.P., Sviripa V.M., Wyrebek P., Mohler J. L., Fiandalo M.V., Liu C., Frasinyuk M.S., Watt D.S.. A Direct Synthesis of 2-(?-Carboxyalkyl)-isoflavones from ortho-Hydroxylated Deoxybenzoins. Eur. J. Org. Chem.- 2018. – Vol. 39. – P. 5460- 5463.
52. Bondarenko S.P., Frasinyuk M.S., Mrug G.P., Vinogradova V.I., Khilya V.P.. Synthesis of Isoflavone-Anabasine Conjugates. Chem. Nat. Comp.- 2018.- Vol. 54, № 6. – P. 1068-1071 https://dx.doi.org/10.1007/s10600-018-2557-y.
53. Tsygankova V.A., Andrusevich Ya.V., Shtompel O.I., Solomyanny R.M., Hurenko A.O., Frasinyuk M.S., Mrug G.P., Shablykin O.V., Pilyo S.G., Kornienko A.M., Brovarets V.S.. Study of auxin-like and cytokinin-like activities of derivatives of pyrimidine, pyrazole, isoflavones, pyridine, oxazolopyrimidine and oxazole on haricot bean and pumpkin plants. Intern. J. Chem. Tech. Res.- 2018. -Vol. 11, № 10. – P. 174-190.
54. Nizhenkovska E.V., Sedko K.V., Golovchenko O.I., Golovchenko O.V.. Efficiency of the application of the 1,3-oxazole-4-ylphosphonic acid derivative on the substained arterial hypertension model in rats. Curr. Topics Pharmacology.- 2018. – Vol. 22, № 63. – P. 63-68.
55. Velihina Ye.S., Kachaeva M.V., Pilyo S.G., Mitiukhin O.P., Zhirnov V.V., Brovarets V.S.. Synthesys, characterization and in vitro anticancer evaluation of 7-(1,4-diazepan)substituted [1,3]oxazolo[4,5]pyrimidines. Chem. Res. J.- 2018 Doi:10.1007/s00044-018-2265-y.
56. Pavlenko O.L., Brusentsov V.A., Dmytrenko O.P., Kulish M.P., Sendiuk V.A., Kobzar P.Yu., Strelchuk V.V., Slominskyi Yu.L., Kurdiukov B.V., Kachkovskyi O.D., Prostota Ya.O.. Spectral and Quantum-Chemical Study of Interaction Between Fullerenes and Squaraine Dyes. Nanosistemi, Nanomateriali, Nanotehnologii.- 2018. – Vol.16, № 1. – P. 31–40. https://www.imp.kiev.ua/nanosys/ua/articles/2018/1/nano_vol16_iss1_p0031p0040_2018_abstract.html
57. Pavlenko E.L., Sendiuk V.A., Brusentsov V.A., Dmytrenko O.P., Kulish M.P., Obernihina N.V., Prostota Y.O., Kachkovsky O.D., Brovarets V.S.. Quantum-Chemical Study of Acceptor Properties of Fullerene and Its Bridge Derivatives. Nanosistemi, Nanomateriali, Nanotehnologii.- 2018. – Vol. 16, № 2. – P. 389-401 https://www.imp.kiev.ua/nanosys/ua/articles/2018/2/nano_vol16_iss2_p0389p0401_2018_abstract.html
58. Shokol T.V., Gorbulenko N.V., Frasinyuk M.S., Khilya V.P.. Furo[2,3-h]chromones and pyrano[2’,3’:5,6]chromeno[4,3-b]pyridines based on natural isoflavones. Chem. Nat. Comp.- 2018. – Vol. 54, № 6. – Р. 1065-1067 https://dx.doi.org/10.1007/s10600-018-2556-z.
59. Popova A.V., Bondarenko S.P., Frasinyuk M.S.. Synthesis and aminomethylation of regioisomeric 6-hydroxy-4-methyl- and 4-hydroxy-6-methylaurones. Chem. Heter. Comp.- 2018. – Vol. 54, № 9. – P. 832- 839.
60. Bondarenko S.P., Frasinyuk M.S.. Observations from aminomethylation of 7-substituted 6-hydroxyaurones. Chem. Heter. Comp.- 2018. – Vol. 54, № 8. – P. 765-762.
61. Shokol T.V., Abdullaev E.N., Gorbulenko N.V., Frasinyuk M.S., Khilya V.P.. Synthesis and modification of 6-thiazolyl-4-methylumbelliferone. Chem. Nat. Comp. 2018. – Vol. 54, №3. – P. 439-442.
62. Tolmachova K., Moroz Y., Konovets A., Platonov M., Vasylchenko O., Borysko P., Zozulya S., Gryniukova A., Bogolubsky A., Pipko S., Mykhailiuk P., Brovarets V., Grygorenko O. . (Chlorosulfonyl)benzenesulfonyl Fluorides—Versatile Building Blocks for Combinatorial Chemistry: Design, Synthesis and Evaluation of a Covalent Inhibitor Library. ACS Comb. Sci.- 2018. – Vol. 20, № 11. – P. 672-680.
63. Adejuwon A.O., Tsygankova V.A., Alonge O.. Effect of cultivation conditions on activity of ?-amylase from a tropical strain Aspergillus Flavus Link. J. Microbiol. Biotechnol. Food Sci.- 2018. -Vol.7, № 6. – P. 571-575.
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2017 р.

1 . V. Tsygankova, Y. Andrusevich, O. Shtompel, O. Romaniuk, M. Yaikova, A. Hurenko, R. Solomyanny, E. Abdurakhmanova, S. Klyuchko, O. Holovchenko, O. Bondarenko, V. Brovarets Application of Synthetic Low Molecular Weight Heterocyclic Compounds Derivatives of Pyrimidine, Pyrazole and Oxazole in Agricultural Biotechnology as a New Plant Growth Regulating Substances. // Int. J. Med. Biotechnol. & Genetics. – 2017. – S2: 002.– P. 10-32.
2 . Tsygankova V.A., Andrusevich Ya.V., Shtompel O.I., Kopich V.M., Pilyo S.G., Prokopenko V.M, Kornienko A.M, Brovarets V.S. Intensification of Vegetative Growth of Cucumber by Derivatives of [1,3]oxazolo[5,4-d]pyrimidine and N-sulfonyl substituted of 1,3-oxazole. // Research Journal of Life Sciences, Bioinformatics, Pharmaceutical, and Chemical Sciences(RJLBPCS). – 2017. – V.3, № 4. – P. 107 – 122. DOI://doi.org/10.26479/rjlbpcs
3 . Victoria Tsygankova, Elena Shysha, Anatoly Galkin, Lyudmila Biliavska, Galina Iutynska, Alla Yemets, Yaroslav Blume Impact of Microbial Biostimulants on Induction of Callusogenesis and Organogenesis in the Isolated Tissue Culture of Wheat in vitro. // J. Med. Plants. Stud. – 2017. – V. 5, Issue 3. – P. 155-164.
4 . V.Kovalishyn,V.Brovarets,V.Blagodatnyi,I. Kopernyk,D. Hodyna,S.Chumachenko,O.Shablykin,O. Kozachenko,M. Vovk,M.Barus,M. Bratenko, L.Metelytsia QSAR studies, synthesis and antibacterial assessment of new inhibitors against multidrug-resistant Mycobacterium tuberculosis. // Current Drug Discovery Technologies.- 2017.- V.14, N.1 .- P. 25-38.
5 . Maria M. Trush, Ivan V. Semenyuta, Sergey I. Vdovenko, Sergiy P. Rogalsky, Evgeniya O. Lobko, Larisa O. Metelytsia Synthesis, spectroscopic and molecular docking studies of imidazolium and pyridinium based ionic liquids with HSA as potential antimicrobial agents. // Journal of Molecular Structure.-V.1137, 5.- 2017.- P. 692–699
6 . Protasov Al., Bardeau JF., Morozovskaya I., Boretska M., Cherniavska T., Petrus L., Tarasyuk O., Metelytsia L., Kopernyk I., Kalashnikova L., Dzhuzha O., Rogalsky S. New promising antifouling agent based on polymeric biocide polyhexamethylene guanidine molybdate. // Environ. Toxicol Chem. 2017.- V. 36(9).- P. 2543-2551.
7 . Soares A., Estevao M.S., Marques M.M.B., Kovalishyn V., A.R.S. Latino D., Aires-de-Sousa J., Ramos J., Viveiros M., Martins F. Synthesis and Biological Evaluation of Hybrid 1,5- and 2,5-Disubstituted Indoles as Potentially New Antitubercular Agents. // Medicinal chemistry.- 2017.- 13 (5), Р. 439-447
8 . Kovalishyn V., Abramenko N., Kopernyk I., Charochkina L., Metelytsia L., Tetko I.V., Peijnenburg W.,Kustov L. Modelling the toxicity of a large set of metal and metal oxide nanoparticles using the OCHEM platform. // Food and Chemical Toxicology.- 2017. – 17. – S.0278-6915.doi: 10.1016/ j.fct.2017.08.008.
9 . H.S Sayiner, A. A.S. Abdalrahm, M. A. Basaran, V. Kovalishyn, F. Kandemirli The Quantum Chemical and QSAR Studies on Acinetobacter Baumannii Oxphos Inhibitors. // Medicinal Chemistry.- 2017.-V.13, DOI : 10.2174/1573406413666171002124408
10 . Абдурахманова Э.Р., Пильо C.Г., Кондратюк К.М., Головченко А.В., Броварец В.С. 1,3-Оксазол¬содер¬жащие про¬извод¬ные цитизина. // ЖОХ.- 2017.- Т.87, №2.- С.268-276.
11 . Kolodiazhnyi O.I.,Kolodiazhna A.O. Nucleophilic substitution at phosphorus: stereochemistry and Mechanisms. // Tetrahedron: Asymmetry. 2017.- 28,N11; doi.org/10.1016/ j.tetasy.2017.10.02
12 . Kolodiazhnyi O.I., Kolodiazhna A.O. Stereochemistry of nucleophilic substitution at trivalent phosphorus. // Phosphorus, Sulfur, and Silicon and the Related Elements.- 2017.- V. 192, N 6.- P. 621-633
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32. Korzh R. Supercritical water as nanomedium for gasification of lignite-water suspension / R. Korzh, V. Bortyshevskyi // NanoScale Res. Lett. — 2016. — 11, №1. — P. 255–263.
33. Belik M. Y. Resolution of fluorinated aminophosphonic acid enantiomers by precolumn derivatization with following reverse phase liquid chromatography / M. Y. Belik, O. Yegorov, A. E. Sorochinsky, V. P. Kukhar // Phosphorus, Sulfur, and Silicon — 2016. — 191, №3. — P. 423–429.
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35. Povolotskii M. I. Molecular and electronic structure of 1,3,2-diazaphosphinine derivatives / M. I. Povolotskii, O. V. Shablykin, E. B. Rusanov, A. B. Rozhenko // Phosporus, Sulfur, and Silicon. — 2016. — 191, №3. — P. 399–404.
36. Derevyanchuk M. Brassinosteroid-induced de novo protein synthesis in zea mays under salinity and bioinformatic approach for identification of heat shock proteins / M. Derevyanchuk, R. Litvinovskaya, V. Khripach, V. Kravets // Plant Growth Regul. — 2016. — 78, №3. — P. 297–305.
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50. Mikhaylov S. The PANI-DBSA content and dispersing solvent as influencing parameters in sensing performances of TiO 2/PANI-DBSA hybrid nanocomposites to ammonia / S. Mikhaylov, N. A. Ogurtsov, N. Redon[et al.] // RSC Adv. — 2016. — 6, №86. — P. 82625–82634.
51. Tsygankova V. Study of auxin, cytokinin and gibberellin-like activity of heterocyclic compounds derivatives of pyrimidine, pyridine, pyrazole and isoflavones / V. Tsygankova, Y. Andrusevich, O. Shtompel[et al.] // 2016. — 4, №12. — P. 29–44.
52. Tsygankova V. A. Stimulating effect of five and six-membered heterocyclic compounds on seed germination and vegetative growth of maize (Zea mays L.) / V. A. Tsygankova, Y. Andrusevich, O. Shtompel[et al.] // 2016. — 1, №4. — P. 1–14.

2015 р.

1. Borisova T. Synthesis of new fluorinated analogs of gaba, pregabalin bioisosteres, and their effects on [3H]gaba uptake by rat brain nerve terminals / T. Borisova, N. Pozdnyakova, E. Shaitanova[et al.] // Bioorg. Med. Chem. — 2015. — 23, №15. — P. 4316–4323.
3. Chernykh A. V. Synthesis and physicochemical properties of 3-fluorocyclobutylamines / A. V. Chernykh, D. S. Radchenko, A. V. Chernykh[et al.] // Eur. J. Org. Chem. — 2015. — 2015, №29. — P. 6466–6471.
4. Chumachenko S. A. Interaction of 5-(morpholin-4-yl)-2-(4-phthal-imidobutyl)- and 5-(morpholin-4-yl)-2-(5-phthal-imidopentyl)-1,3-oxazole-4-carbonitriles with hydrazine hydrate / S. A. Chumachenko, O. V. Shablykin, V. S. Brovarets // Chem Heterocycl Comp. — 2015. — 50, №12. — P. 1727–1730.
5. Dahi A. Water sorption properties of room-temperature ionic liquids over the whole range of water activity and molecular states of water in these media / A. Dahi, K. Fatyeyeva, C. Chappey[et al.] // RSC Adv. — 2015. — 5, №94. — P. 76927–76938.
6. Derevyanchuk M. Effect of 24-epibrassinolide on arabidopsis thaliana alternative respiratory pathway under salt stress / M. Derevyanchuk, R. Litvinovskaya, V. Khripach[et al.] // Acta Physiol Plant. — 2015. — 37, №10. — P. 215.
7. Frasinyuk M. S. Synthesis and tautomerization of hydroxylated isoflavones bearing heterocyclic hemi-aminals / M. S. Frasinyuk, S. P. Bondarenko, V. P. Khilya[et al.] // Org. Biomol. Chem. — 2015. — 13, №4. — P. 1053–1067.
8. Frasinyuk M. S. Development of 6H-chromeno[3,4-c]pyrido[3′,2′:4,5]thieno[2,3-e]pyridazin-6-ones as par-4 secretagogues / M. S. Frasinyuk, S. P. Bondarenko, V. M. Sviripa[et al.] // Tetrahedron Lett. — 2015. — 56, №23. — P. 3382–3384.
9. Frasinyuk M. S. Application of mannich bases to the synthesis of hydroxymethylated isoflavonoids as potential antineoplastic agents / M. S. Frasinyuk, G. P. Mrug, S. P. Bondarenko[et al.] // Org. Biomol. Chem. — 2015. — 13, №46. — P. 11292–11301.
10. Grynko D. O. Multifunctional role of nanostructured cds interfacial layers in hybrid solar cells / D. O. Grynko, O. M. Fedoryak, P. S. Smertenko[et al.] // J Nanosci Nanotechnol. — 2015. — 15, №1. — P. 752–758.
11. Hamouda Z. Dual-band elliptical planar conductive polymer antenna printed on a flexible substrate / Z. Hamouda, J. L. Wojkiewicz, A. A. Pud[et al.] // IEEE Transactions on Antennas and Propagation — 2015. — 63, №12. — P. 5864–5867.
12. Kalachova T. Importance of phosphoinositide-dependent signaling pathways in the control of gene expression in resting cells and in response to phytohormones / T. Kalachova, V. Kravets, A. Zachowski, E. Ruelland // Plant Signal Behav. — 2015. — 10, №5. — P. e1019983.
13. Kobzar O. L. Phosphonate derivatives of tetraazamacrocycles as new inhibitors of protein tyrosine phosphatases / O. L. Kobzar, M. V. Shevchuk, A. N. Lyashenko[et al.] // Org. Biomol. Chem. — 2015. — 13, №27. — P. 7437–7444.
14. Kobzar O. L. Polycarboxylic fullerene derivatives as protein tyrosine phosphatase inhibitors / O. L. Kobzar, V. V. Trush, V. Y. Tanchuk[et al.] // Mendeleev Comm. — 2015. — 25, №3. — P. 199–201.
15. Kolodiazhna A. O. Synthesis and properties of four-membered phosphorus heterocycles-2-fluoro-1,2lambda5-oxaphosphetanes / A. O. Kolodiazhna, O. I. Kolodiazhnyi // Phosph., Sulfur, Silicon Relat. Elem. — 2015. — 190, №12. — P. 2232–2245.
16. Kolodiazhna O. O. Synthesis of anti-cis-phosphiranes / O. O. Kolodiazhna, O. I. Kolodiazhnyi // Phosph., Sulfur, Silicon Relat. Elem. — 2015. — 190, №7. — P. 1192–1200.
20. Kondratov I. S. Synthesis of trifluoromethyl-containing polysubstituted aromatic compounds by Diels–Alder reaction of ethyl 3-benz­amido-2-oxo-6-(trifluoromethyl)-2H-pyran-5-carboxylate / I. S. Kondratov, N. A. Tolmachova, V. G. Dolovanyuk[et al.] // Eur. J. Org. Chem. — 2015. — 2015, №11. — P. 2482–2491.
21. Kovalishyn V. Efficient variable selection batch pruning algorithm for artificial neural networks / V. Kovalishyn, G. Poda // Chemometrics and Intelligent Lab. Sys. — 2015. — 149, Part B. — P. 10–16.
23. Lukashuk O. I. Introduction of chiral 2-(aminoalkyl) substituents into 5-amino-1,3-oxazol-4-ylphosphonic acid derivatives and their use in phosphonodipeptide synthesis / O. I. Lukashuk, E. R. Abdurakhmanova, K. M. Kondratyuk[et al.] // RSC Adv. — 2015. — 5, №15. — P. 11198–11206.
24. Mikhaylov S. Ammonia/amine electronic gas sensors based on hybrid polyaniline–tio2 nanocomposites. the effects of titania and the surface active doping acid / S. Mikhaylov, N. Ogurtsov, Y. Noskov[et al.] // RSC Adv. — 2015. — 5, №26. — P. 20218–20226.
25. Mkrtchyan G. Molecular mechanisms of the non-coenzyme action of thiamin in brain: biochemical, structural and pathway analysis / G. Mkrtchyan, V. Aleshin, Y. Parkhomenko[et al.] // Sci Rep. — 2015. — 5. — P. 12583.
26. Ogurtsov N. A. Effect of multiwalled carbon nanotubes on the kinetics of the aniline polymerization: the semi-quantitative ocp approach / N. A. Ogurtsov, Y. V. Noskov, A. A. Pud // J. Phys. Chem. B. — 2015. — 119, №15. — P. 5055–5061.
27. Pud A. “Anion-chromic” interactions of emeraldine base with hydroxide and halide anions in the solid polymer matrix / A. Pud, I. Duboriz, Y. Piryatinski, O. Dimitriev // Synthetic Metals. — 2015. — 209. — P. 232–239.
28. Ruelland E. Role of phospholipid signalling in plant environmental responses / E. Ruelland, V. Kravets, M. Derevyanchuk[et al.] // Environmental and Experimental Botany. — 2015. — 114. — P. 129–143.
29. Tanchuk V. Y. A new scoring function for molecular docking based on autodock and autodock vina / V. Y. Tanchuk, V. O. Tanin, A. I. Vovk, G. Poda // Curr Drug Discov Technol. — 2015. — 12, №3. — P. 170–178.
30. Tarasevych A. V. High temperature sublimation of alpha-amino acids: a realistic prebiotic process leading to large enantiomeric excess / A. V. Tarasevych, A. E. Sorochinsky, V. P. Kukhar, J.-C. Guillemin // Chem. Commun. — 2015. — 51, №32. — P. 7054–7057.
31. Tarasevych A. V. Attrition-induced spontaneous chiral amplification of the gamma polymorphic modification of glycine / A. V. Tarasevych, A. E. Sorochinsky, V. P. Kukhar[et al.] // Cryst. Eng. Comm. — 2015. — 17, №7. — P. 1513–1517.
32. Trush V. V. Phosphonate monoesters on a thiacalix[4]arene framework as potential inhibitors of protein tyrosine phosphatase 1B / V. V. Trush, S. G. Kharchenko, V. Y. Tanchuk[et al.] // Org. Biomol. Chem. — 2015. — 13, №33. — P. 8803–8806.
33. Tsygankova V. Genetic control and phytohormonal regulation of plant embryogenesis / V. Tsygankova // Int. J. Medical Biotechnology Genetics (I)MBG — 2015. — P. 9–20.
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35. Zahanich I. Phenoxymethyl 1,3-oxazoles and 1,2,4-oxadiazoles as potent and selective agonists of free fatty acid receptor 1 (GPR40) / I. Zahanich, I. Kondratov, V. Naumchyk[et al.] // Bioorg. Med. Chem. Lett. — 2015. — 25, №16. — P. 3105–3111.
37. Zhirnov V. V. The osmotic resistance, and zeta potential responses of human erythrocytes to transmembrane modification of Ca2+ fluxes in the presence of the imposed low rate radiation field of 90Sr / V. V. Zhirnov, I. N. Iakovenko // Int. J. Radiat. Biol. — 2015. — 91, №1. — P. 117–126.

2014 р.

1. Acena J. L. Asymmetric synthesis of alpha-amino acids via homologation of Ni(II) complexes of glycine schiff bases. Part 3: michael addition reactions and miscellaneous transformations / J. L. Acena, A. E. Sorochinsky, V. Soloshonok // Amino Acids. – 2014. – 46, №9. – P. 2047-2073.
2. Bondarenko S. P. Synthesis of 4-aryl-3-[2-hydroxy-4-(2-cytisin-12-ylethoxy)phenyl]pyrazoles / S. P. Bondarenko, M. S. Frasinyuk, V. I. Vinogradova, V. P. Khilya // Chem. Nat. Compd. – 2014. – 50, №5. – P. 889-891.
3. Brandmaier S. The qspr-thesaurus: the online platform of the cadaster project / S. Brandmaier, W. Peijnenburg, M. K. Durjava[et al.] // Altern Lab Anim. – 2014. – 42, №1. – P. 13-24.
4. Dahi A. Supported ionic liquid membranes for water and volatile organic compounds separation: sorption and permeation properties / A. Dahi, K. Fatyeyeva, D. Langevin[et al.] // Journal of Membrane Science. – 2014. – 458. – P. 164-178.
5. Dahi A. Polyimide/ionic liquid composite membranes for fuel cells operating at high temperatures / A. Dahi, K. Fatyeyeva, D. Langevin[et al.] // Electrochimica Acta. – 2014. – 130. – P. 830-840.
6. Derevyanchuk M. V. Influence of brassinosteroids on plant cell alternative respiration pathway and antioxidant systems activity under abiotic stress conditions / M. V. Derevyanchuk, O. I. Grabelnyh, R. P. Litvinovskaya[et al.] // Biopolym. Cell. – 2014. – 30, №6. – P. 436-442.
7. D. Romanenko V. Progress in the development of pyrophosphate bioisosteres: synthesis and biomedical potential of 1-fluoro- and 1,1-difluoromethylene-1,1-bisphosphonates / V. D. Romanenko, V. P. Kukhar // Curr. Org. Chem. – 2014. – 18, №11. – P. 1491-1512.
8. Duboriz I. Polyaniline/poly(ethylene terephthalate) film as a new optical sensing material / I. Duboriz, A. Pud // Sensors and Actuators B: Chemical. – 2014. – 190. – P. 398-407.
9. Frasinyuk M. S. Pentapeptide boronic acid inhibitors of mycobacterium tuberculosis MYCP1 protease / M. S. Frasinyuk, S. Kwiatkowski, J. M. Wagner[et al.] // Bioorg. Med. Chem. Lett. – 2014. – 24, №15. – P. 3546-3548.
10. Goushcha A. O. Self-organization and coherency in biology and medicine / A. O. Goushcha, T. O. Hushcha, L. N. Christophorov, M. Goldsby // Open J. Bioph. – 2014. – 04, №04. – P. 119.
11. Grynko D. O. Hybrid solar cells based on CDS nanowire arrays / D. O. Grynko, O. M. Fedoryak, P. S. Smertenko[et al.] // Adv. Mat. Res. 2014. – 854. – P. 75-82.
12. Gurenko A. O. Synthesis of novel pyrazolo[3,4-d][1,2,3]triazines / A. O. Gurenko, B. M. Khutova, S. V. Klyuchko[et al.] // Chem. Heterocycl Comp. – 2014. – 50, №4. – P. 528-536.
13. Kaminskyy D. Isothiocoumarin-3-carboxylic acid derivatives: synthesis, anticancer and antitrypanosomal activity evaluation / D. Kaminskyy, A. Kryshchyshyn, I. Nektegayev[et al.] // Eur. J. Med. Chem. – 2014. – 75. – P. 57-66.
14. Kobelev S. M. Macrobicyclic and macrotricyclic derivatives of N,N’,N”,N”’-tetrasubstituted cyclen and cyclam / S. M. Kobelev, A. D. Averin, A. K. Buryak[et al.] // Heterocycles – 2014. – 90, №2. – P. 989-1017.
15. Kobzar O. L. Fullerene derivatives as a new class of inhibitors of protein tyrosine phosphatases / O. L. Kobzar, V. V. Trush, V. Y. Tanchuk[et al.] // Bioorg. Med. Chem. Lett. – 2014. – 24, №14. – P. 3175-3179.
16. Kolodiazhnyi O. I. Asymmetric catalysis as a method for the synthesis of chiral organophosphorus compounds / O. I. Kolodiazhnyi, V. P. Kukhar, A. O. Kolodiazhna // Tetrahedron: Asymmetry. – 2014. – 25, №12. – P. 865-922.
17. Kolodiazhnyi O. I. Advances in asymmetric hydrogenation and hydride reduction of organophosphorus compounds / O. I. Kolodiazhnyi // Phosphorus, Sulfur, and Silicon – 2014. – 189, №7-8. – P. 1102-1131.
18. Kolodiazhnyi O. I. Recent advances in asymmetric synthesis of р-stereogenic phosphorus compounds / O. I. Kolodiazhnyi // J.-L. Montchamp. – Springer International Publishing, 2014. – P. 161-236.
21. Kondratov I. S. Diels-alder reaction of ethyl 3-benzamido-2-oxo-6-(trifluoromethyl)-2h-pyran-5-carboxylate with alkoxyalkenes as an effective approach to trifluoromethyl-containing 3-aminobenzoic acid derivatives / I. S. Kondratov, N. A. Tolmachova, V. G. Dolovanyuk[et al.] // Eur. J. Org. Chem. – 2014. – 2014, №12. – P. 2443-2450.
22. Kornienko A. N. Reaction of 2-aryl-4-cyano-1,3-oxazole-5-sulfonyl chlorides with 5-amino-1H-pyrazoles and 5-amino-1H-1,2,4-triazole / A. N. Kornienko, S. G. Pil’o, A. P. Kozachenko[et al.] // Chem Heterocycl Comp. – 2014. – 50, №1. – P. 76-86.
27. Kovalishyn V. Qsar studies, design, synthesis and antimicrobial evaluation of azole derivatives / V. Kovalishyn, I. Kopernyk, S. Chumachenko[et al.] // Computational Biology and Bioinformatics. – 2014. – 2, №2. – P. 25.
28. Kovalishyn V. Prediction of thrombin and factor XA inhibitory activity with associative neural networks / V. Kovalishyn, V. Tanchuk, I. Kopernyk[et al.] // Curr Comput Aided Drug Des. – 2014. – 10, №3. – P. 259-265.
29. Kucher O. V. Enzyme-catalyzed kinetic resolution of 2,2,2-trifluoro-1-(heteroaryl)ethanols: experimental and docking studies / O. V. Kucher, A. O. Kolodiazhnaya, O. B. Smolii[et al.] // Eur. J. Org. Chem. – 2014. – 2014, №34. – P. 7692-7698.
30. Kucher O. V. Enzymatic resolution of chroman-4-ol and its core analogues with burkholderia cepacia lipase / O. V. Kucher, A. O. Kolodyazhnaya, O. B. Smolii[et al.] // Tetrahedron: Asymmetry. – 2014. – 25, №6-7. – P. 563-567.
31. Kukharenko O. Promising low cost antimicrobial composite material based on bacterial cellulose and polyhexamethylene guanidine hydrochloride / O. Kukharenko, J.-F. Bardeau, I. Zaets[et al.] // European Polymer Journal. – 2014. – 60. – P. 247-254.
32. Lioshina L. G. Plant regeneration from hairy roots and calluses of periwinkle vinca minor l. and foxglove purple digitalis purpurea l. / L. G. Lioshina, O. V. Bulko // Cytol. Genet. – 2014. – 48, №5. – P. 302-307.
33. Maestro M. A. Chiral N(H)-tbu and N(H)-ad NiII complexes of glycine schiff bases: deduction of a mode of kinetic diastereoselectivity / M. A. Maestro, F. Avecilla, A. E. Sorochinsky[et al.] // Eur. J. Org. Chem. – 2014. – 2014, №20. – P. 4309-4314.
34. Martins F. Design, synthesis and biological evaluation of novel isoniazid derivatives with potent antitubercular activity / F. Martins, S. Santos, C. Ventura[et al.] // Eur. J. Med. Chem – 2014. – 81. – P. 119-138.
35. Pokholenko I. O. Development and characterization of porous functionalized collagen scaffolds for delivery of fgf-2 / I. O. Pokholenko, M. D. Chetyrkina, L. V. Dubey[et al.] // Biopolym. Cell. – 2014. – 30, №3. – P. 216-222.
36. Pokotylo I. Plant phosphoinositide-dependent phospholipases c: variations around a canonical theme / I. Pokotylo, Y. Kolesnikov, V. Kravets[et al.] // Biochimie. – 2014. – 96. – P. 144-157.
37. Pokotylo I. V. Influence of 24-epibrassinolide on lipid signalling and metabolism in brassica napus / I. V. Pokotylo, S. V. Kretynin, V. A. Khripach[et al.] // Plant Growth Regul. – 2014. – 73, №1. – P. 9-17.
38. Prokopenko V. Design and synthesis of new potent inhibitors of farnesyl pyrophosphate synthase / V. Prokopenko, V. Kovalishyn, M. Shevchuk[et al.] // Curr Drug Discov Technol. – 2014. – 11, №2. – P. 133-144.
39. Rogalsky S. Antimicrobial properties and thermal stability of polycarbonate modified with 1-alkyl-3-methylimidazolium tetrafluoroborate ionic liquids / S. Rogalsky, K. Fatyeyeva, L. Lyoshina[et al.] // J. Appl. Polym. Sci. – 2014. – 131, №7. – P. n/a-n/a.
40. Rogalsky S. P. Antimicrobial polycarbonates for biomedical applications / S. P. Rogalsky, O. V. Moshynets, L. G. Lyoshina, O. P. Tarasyuk // EPMA J. – 2014. – 5, №Suppl 1. – P. A133.
41. Shaitanova E. N. Synthesis of enantiomerically pure 4-polyfluoromethyl-4-hydroxy-homoprolines by intramolecular cyclization of 6-amino-5-polyfluoromethyl-hex-2-enoic acids / E. N. Shaitanova, I. I. Gerus, V. P. Kukhar, G. Haufe // J. Fluorine Chem. – 2014. – 160. – P. 8-11.
42. Shibata N. Asymmetric mannich reaction between (S)-N-(tert-butanesulfinyl)-3,3,3-trifluoroacetaldimine and malonic acid derivatives. stereodivergent synthesis of (R)- and (S)-3-amino-4,4,4-trifluorobutanoic acids / N. Shibata, T. Nishimine, N. Shibata[et al.] // Org. Biomol. Chem. – 2014. – 12, №9. – P. 1454-1462.
43. Shishkina S. V. Crystal structure of (S)-1-(1,3-benzo­thia­zol-2-yl)-2,2,2-tri­fluoro­ethanol / S. V. Shishkina, O. V. Kucher, A. O. Kolodiazhnaya[et al.] // Acta Cryst E. – 2014. – 70, №9. – P. o946-o946.
44. Tsygankova V. A. Impact of new microbial PR/PGP inducers on increase of resistance to parasitic nematode of wild and rnai transgenic rape plants / V. A. Tsygankova, L. O. Biliavska, Y. V. Andrusevich[et al.] // Adv. Biosc. Bioeng. 2014. – 2, №1.
45. Vasylyshyn R. Y. Efficient synthesis of 1,3,5-benzotriazocines from tetrachloro-2-aza-1,3-dienes / R. Y. Vasylyshyn, B. A. Demydchuk, E. B. Rusanov, V. S. Brovarets // Synthetic Commun. – 2014. – 44, №5. – P. 714-719.
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48. Zelisko N. Crotonic, cynnamic, and propiolic acids motifs in the synthesis of thiopyrano[2,3-d][1,3]thiazoles via hetero-diels-alder reaction and related tandem processes / N. Zelisko, D. Atamanyuk, O. Vasylenko[et al.] // Tetrahedron. – 2014. – 3, №70. – P. 720-729.

2013 р.

1. Acena J. L. Unconventional preparation of racemic crystals of isopropyl 3,3,3-trifluoro-2-hydroxypropanoate and their unusual crystallographic structure: the ultimate preference for homochiral intermolecular interactions / J. L. Acena, A. E. Sorochinsky, T. Katagiri, V. A. Soloshonok // Chem. Commun. — 2013. — 49, №4. — P. 373–375.
2. Acena J. L. Synthesis of fluorine-containing alpha-amino acids in enantiomerically pure form via homologation of Ni(II) complexes of glycine and alanine schiff bases / J. L. Acena, A. E. Sorochinsky, H. Moriwaki[et al.] // Journal of Fluorine Chemistry. — 2013. — 155. — P. 21–38.
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